| Year |
Citation |
Score |
| 2022 |
Koppaka A, Kirkland JK, Periana RA, Ess DH. Experimental Demonstration and Density Functional Theory Mechanistic Analysis of Arene C-H Bond Oxidation and Product Protection by Osmium Tetroxide in a Strongly Basic/Nucleophilic Solvent. The Journal of Organic Chemistry. PMID 36191170 DOI: 10.1021/acs.joc.2c01159 |
0.518 |
|
| 2021 |
Chen SS, Koppaka A, Periana RA, Ess DH. Theory and Experiment Demonstrate that Sb(V)-Promoted Methane C-H Activation and Functionalization Outcompete Superacid Protonolysis in Sulfuric Acid. Journal of the American Chemical Society. 143: 18242-18250. PMID 34665603 DOI: 10.1021/jacs.1c08170 |
0.505 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/Acs.Organomet.0C00120 |
0.802 |
|
| 2019 |
King CR, Holdaway A, Durrant G, Wheeler J, Suaava L, Konnick MM, Periana RA, Ess DH. Supermetal: SbF-mediated methane oxidation occurs by C-H activation and isobutane oxidation occurs by hydride transfer. Dalton Transactions (Cambridge, England : 2003). PMID 31693026 DOI: 10.1039/C9Dt03564H |
0.75 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/Acs.Organomet.9B00246 |
0.815 |
|
| 2018 |
Koppaka A, Park T, Hashiguchi B, King C, Konnick M, Ess D, Periana R. Selective C-H Functionalization of Methane and Ethane by a Molecular Sb(V) Complex. Angewandte Chemie (International Ed. in English). PMID 30589173 DOI: 10.1002/Anie.201809159 |
0.815 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/Acs.Organomet.8B00418 |
0.817 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/Acs.Organomet.8B00371 |
0.76 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.767 |
|
| 2017 |
Periana RA. Comment on "Selective anaerobic oxidation of methane enables direct synthesis of methanol". Science (New York, N.Y.). 358. PMID 29026016 DOI: 10.1126/Science.Aan5970 |
0.403 |
|
| 2017 |
Gunsalus NJ, Koppaka A, Park SH, Bischof SM, Hashiguchi BG, Periana RA. Homogeneous Functionalization of Methane. Chemical Reviews. PMID 28459540 DOI: 10.1021/Acs.Chemrev.6B00739 |
0.811 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/Acscatal.6B00226 |
0.801 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/Acs.Organomet.6B00475 |
0.798 |
|
| 2015 |
Gustafson SJ, Fuller JT, Devarajan D, Snyder J, Periana RA, Hashiguchi BG, Konnick MM, Ess DH. Contrasting Mechanisms and Reactivity of Tl(III), Hg(II), and Co(III) for Alkane C-H Functionalization Organometallics. 34: 5485-5495. DOI: 10.1021/Acs.Organomet.5B00849 |
0.827 |
|
| 2014 |
Coggins MK, Méndez MA, Concepcion JJ, Periana RA, Meyer TJ. Selective electrocatalytic oxidation of a re-methyl complex to methanol by a surface-bound Ru(II) polypyridyl catalyst. Journal of the American Chemical Society. 136: 15845-8. PMID 25325162 DOI: 10.1021/Ja507979C |
0.533 |
|
| 2014 |
Konnick MM, Hashiguchi BG, Devarajan D, Boaz NC, Gunnoe TB, Groves JT, Gunsalus N, Ess DH, Periana RA. Selective CH functionalization of methane, ethane, and propane by a perfluoroarene iodine(III) complex. Angewandte Chemie (International Ed. in English). 53: 10490-4. PMID 25131994 DOI: 10.1002/Anie.201406185 |
0.833 |
|
| 2014 |
Konnick MM, Bischof SM, Yousufuddin M, Hashiguchi BG, Ess DH, Periana RA. A mechanistic change results in 100 times faster CH functionalization for ethane versus methane by a homogeneous Pt catalyst. Journal of the American Chemical Society. 136: 10085-94. PMID 24925375 DOI: 10.1021/Ja504368R |
0.826 |
|
| 2014 |
Fortman GC, Boaz NC, Munz D, Konnick MM, Periana RA, Groves JT, Gunnoe TB. Selective monooxidation of light alkanes using chloride and iodate. Journal of the American Chemical Society. 136: 8393-401. PMID 24866148 DOI: 10.1021/Ja502657G |
0.774 |
|
| 2014 |
Hashiguchi BG, Konnick MM, Bischof SM, Gustafson SJ, Devarajan D, Gunsalus N, Ess DH, Periana RA. Main-group compounds selectively oxidize mixtures of methane, ethane, and propane to alcohol esters. Science (New York, N.Y.). 343: 1232-7. PMID 24626925 DOI: 10.1126/Science.1249357 |
0.817 |
|
| 2014 |
Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J |
0.768 |
|
| 2014 |
Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4Ra90009J |
0.519 |
|
| 2014 |
Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Advances. 4: 35639-35648. DOI: 10.1039/C4Ra06251E |
0.818 |
|
| 2014 |
Stowe RL, Bischof SM, Konnick MM, Hövelmann CH, Leach-Scampavia D, Periana RA, Hashiguchi BG. Making water the exciting way: A classroom demonstration of catalysis Journal of Chemical Education. 91: 550-553. DOI: 10.1021/Ed4006024 |
0.781 |
|
| 2014 |
Konnick MM, Bischof SM, Ess DH, Periana RA, Hashiguchi BG. Base accelerated generation of N2 and NH3 from an osmium nitride Journal of Molecular Catalysis a: Chemical. 382: 1-7. DOI: 10.1016/J.Molcata.2013.10.019 |
0.784 |
|
| 2014 |
Gunsalus NJ, Konnick MM, Hashiguchi BG, Periana RA. Discrete molecular catalysts for methane functionalization Israel Journal of Chemistry. 54: 1467-1480. DOI: 10.1002/Ijch.201300130 |
0.824 |
|
| 2013 |
Mironov OA, Bischof SM, Konnick MM, Hashiguchi BG, Ziatdinov VR, Goddard WA, Ahlquist M, Periana RA. Using reduced catalysts for oxidation reactions: mechanistic studies of the "Periana-Catalytica" system for CH4 oxidation. Journal of the American Chemical Society. 135: 14644-58. PMID 23927450 DOI: 10.1021/Ja404895Z |
0.808 |
|
| 2013 |
Zhou M, Hintermair U, Hashiguchi BG, Parent AR, Hashmi SM, Elimelech M, Periana RA, Brudvig GW, Crabtree RH. Cp* iridium precatalysts for selective C-h oxidation with sodium periodate as the terminal oxidant Organometallics. 32: 957-965. DOI: 10.1021/Om301252W |
0.811 |
|
| 2013 |
Pardue DB, Gustafson SJ, Periana RA, Ess DH, Cundari TR. Computational study of carbon-hydrogen bond deprotonation by alkali metal superbases Computational and Theoretical Chemistry. 1019: 85-93. DOI: 10.1016/J.Comptc.2013.06.041 |
0.517 |
|
| 2013 |
Bischof SM, Hashiguchi BG, Konnick MM, Periana RA. Designing molecular catalysts for selective CH functionalization Topics in Organometallic Chemistry. 44: 195-231. DOI: 10.1007/3418-2012-46 |
0.806 |
|
| 2013 |
Konnick MM, Bischof SM, Periana RA, Hashiguchi BG. The hydroxide-promoted catalytic hydrodefluorination of fluorocarbons by ruthenium in aqueous media Advanced Synthesis and Catalysis. 355: 632-636. DOI: 10.1002/Adsc.201200870 |
0.812 |
|
| 2012 |
Hull JF, Himeda Y, Wang WH, Hashiguchi B, Periana R, Szalda DJ, Muckerman JT, Fujita E. Reversible hydrogen storage using CO2 and a proton-switchable iridium catalyst in aqueous media under mild temperatures and pressures. Nature Chemistry. 4: 383-8. PMID 22522258 DOI: 10.1038/Nchem.1295 |
0.797 |
|
| 2012 |
Hashiguchi BG, Bischof SM, Konnick MM, Periana RA. Designing catalysts for functionalization of unactivated C-H bonds based on the CH activation reaction. Accounts of Chemical Research. 45: 885-98. PMID 22482496 DOI: 10.1021/Ar200250R |
0.837 |
|
| 2012 |
Cheng MJ, Bischof SM, Nielsen RJ, Goddard WA, Gunnoe TB, Periana RA. The para-substituent effect and pH-dependence of the organometallic Baeyer-Villiger oxidation of rhenium-carbon bonds. Dalton Transactions (Cambridge, England : 2003). 41: 3758-63. PMID 22327118 DOI: 10.1039/C2Dt11984F |
0.744 |
|
| 2011 |
Lokare KS, Nielsen RJ, Yousufuddin M, Goddard WA, Periana RA. Iridium complexes bearing a PNP ligand, favoring facile C(sp3)-H bond cleavage. Dalton Transactions (Cambridge, England : 2003). 40: 9094-7. PMID 21833386 DOI: 10.1039/C1Dt10577A |
0.511 |
|
| 2011 |
Liu XY, Lokare KS, Ganesh SK, Gonzales JM, Oxgaard J, Goddard WA, Periana RA. Rhodium complexes bearing tetradentate diamine-bis(phenolate) ligands. Dalton Transactions (Cambridge, England : 2003). 40: 301-4. PMID 21069237 DOI: 10.1039/C0Dt00997K |
0.683 |
|
| 2011 |
Bhalla G, Bischof SM, Ganesh SK, Liu XY, Jones CJ, Borzenko A, Tenn WJ, Ess DH, Hashiguchi BG, Lokare KS, Leung CH, Oxgaard J, Goddard WA, Periana RA. Mechanism of efficient anti-markovnikov olefin hydroarylation catalyzed by homogeneous Ir(iii) complexes Green Chemistry. 13: 69-81. DOI: 10.1039/C0Gc00330A |
0.806 |
|
| 2011 |
Bischof SM, Cheng MJ, Nielsen RJ, Gunnoe TB, Goddard WA, Periana RA. Functionalization of rhenium aryl bonds by O-atom transfer Organometallics. 30: 2079-2082. DOI: 10.1021/Om2002365 |
0.733 |
|
| 2011 |
Young KJH, Mironov OA, Nielsen RJ, Cheng MJ, Stewart T, Goddard WA, Periana RA. Synthesis and characterization of the κ 2-acac- O, O complex Os IV(acac) 2PhCl and study of CH activation with benzene Organometallics. 30: 5088-5094. DOI: 10.1021/Om1010512 |
0.738 |
|
| 2011 |
Young KJH, Lokare KS, Leung CH, Cheng MJ, Nielsen RJ, Petasis NA, Goddard WA, Periana RA. Synthesis of osmium and ruthenium complexes bearing dimethyl (S,S)-2,2′-(pyridine-2,6-diyl)-bis-(4,5-dihydrooxazol-4-carboxylate) ligand and application to catalytic H/D exchange Journal of Molecular Catalysis a: Chemical. 339: 17-23. DOI: 10.1016/J.Molcata.2011.01.029 |
0.643 |
|
| 2011 |
Tenn WJ, Conley BL, Bischof SM, Periana RA. Synthesis, characterization, and C-H activation reactions of novel organometallic O-donor ligated Rh(III) complexes Journal of Organometallic Chemistry. 696: 551-558. DOI: 10.1016/J.Jorganchem.2010.09.021 |
0.802 |
|
| 2011 |
Golisz SR, Brent Gunnoe T, Goddard WA, Groves JT, Periana RA. Chemistry in the center for catalytic hydrocarbon functionalization: An energy frontier research center Catalysis Letters. 141: 213-221. DOI: 10.1007/S10562-010-0499-5 |
0.491 |
|
| 2011 |
Periana RA. New CH activation and functionalization reactions for hydrocarbon oxidation Acs National Meeting Book of Abstracts. |
0.325 |
|
| 2010 |
Hashiguchi BG, Young KJ, Yousufuddin M, Goddard WA, Periana RA. Acceleration of nucleophilic CH activation by strongly basic solvents. Journal of the American Chemical Society. 132: 12542-5. PMID 20734988 DOI: 10.1021/Ja102518M |
0.823 |
|
| 2010 |
Bischof SM, Ess DH, Meier SK, Oxgaard J, Nielsen RJ, Bhalla G, Goddard WA, Periana RA. Benzene C-H bond activation in carboxylic acids catalyzed by O-donor iridium(III) complexes: An experimental and density functional study Organometallics. 29: 742-756. DOI: 10.1021/Om900036J |
0.808 |
|
| 2010 |
Ess DH, Gunnoe TB, Cundari TR, Goddard WA, Periana RA. Ligand lone-pair influence on hydrocarbon C-H activation: A computational perspective Organometallics. 29: 6801-6815. DOI: 10.1021/Om100974Q |
0.736 |
|
| 2010 |
Ess DH, Goddard WA, Periana RA. Electrophilic, ambiphilic, and nucleophilic C-H bond activation: Understanding the electronic continuum of C-H bond activation through transition-state and reaction pathway interaction energy decompositions Organometallics. 29: 6459-6472. DOI: 10.1021/Om100879Y |
0.62 |
|
| 2010 |
Bischof SM, Periana RA, Ringenberg MR, Rauchfuss TB. Iridium Complexes: Oxygen and Carbon Bound Acetylacetonato Iridium(III) Complexes Inorganic Syntheses. 35: 173-178. DOI: 10.1002/9780470651568.ch9 |
0.49 |
|
| 2009 |
Ahlquist M, Nielsen RJ, Periana RA, Goddard WA. Product protection, the key to developing high performance methane selective oxidation catalysts. Journal of the American Chemical Society. 131: 17110-5. PMID 19891471 DOI: 10.1021/Ja903930E |
0.526 |
|
| 2009 |
Ess DH, Nielsen RJ, Goddard WA, Periana RA. Transition-state charge transfer reveals electrophilic, ambiphilic, and nucleophilic carbon-hydrogen bond activation. Journal of the American Chemical Society. 131: 11686-8. PMID 19653684 DOI: 10.1021/Ja902748C |
0.65 |
|
| 2009 |
Young KJ, Oxgaard J, Ess DH, Meier SK, Stewart T, Goddard WA, Periana RA. Experimental realization of catalytic CH4 hydroxylation predicted for an iridium NNC pincer complex, demonstrating thermal, protic, and oxidant stability. Chemical Communications (Cambridge, England). 3270-2. PMID 19587936 DOI: 10.1039/B823303A |
0.797 |
|
| 2009 |
Ahlquist M, Periana RA, Goddard WA. C-H activation in strongly acidic media. The co-catalytic effect of the reaction medium. Chemical Communications (Cambridge, England). 2373-5. PMID 19377690 DOI: 10.1039/B821854D |
0.519 |
|
| 2009 |
Tenn WJ, Conley BL, Hövelmann CH, Ahlquist M, Nielsen RJ, Ess DH, Oxgaard J, Bischof SM, Goddard WA, Periana RA. Oxy-functionalization of nucleophilic rhenium(I) metal carbon bonds catalyzed by selenium(IV). Journal of the American Chemical Society. 131: 2466-8. PMID 19161305 DOI: 10.1021/Ja806814C |
0.808 |
|
| 2009 |
Meier SK, Young KJH, Ess DH, Tenn WJ, Oxgaard J, Goddard WA, Periana RA. Heterolytic benzene C-H activation by a cyclometalated iridium(III) dihydroxo pyridyl complex: synthesis, hydrogen-deuterium exchange, and density functional study Organometallics. 28: 5293-5304. DOI: 10.1021/Om900039S |
0.816 |
|
| 2009 |
Young KJH, Yousufuddin M, Ess DH, Periana RA. Cyclometalation of 6-Phenyl-2,2′-Bipyridine and Iridium: Synthesis, Characterization, and Reactivity Studies Organometallics. 28: 3395-3406. DOI: 10.1021/Om900014H |
0.626 |
|
| 2008 |
Conley BL, Ganesh SK, Gonzales JM, Ess DH, Nielsen RJ, Ziatdinov VR, Oxgaard J, Goddard WA, Periana RA. Facile oxy-functionalization of a nucleophilic metal alkyl with a cis-dioxo metal species via a (2+3) transition state. Angewandte Chemie (International Ed. in English). 47: 7849-52. PMID 18773396 DOI: 10.1002/Anie.200802575 |
0.773 |
|
| 2008 |
Ess DH, Bischof SM, Oxgaard J, Periana RA, Goddard WA. Transition state energy decomposition study of Acetate-Assisted and internal electrophilic substitution C-H Bond activation by (acac-O,O) 2Ir(X) complexes (X = CH 3COO, OH) Organometallics. 27: 6440-6445. DOI: 10.1021/Om8006568 |
0.693 |
|
| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.572 |
|
| 2008 |
Stavropoulos P, Çelenligil-Çetin R, Kiani S, Tapper A, Pinnapareddy D, Paraskevopoulou P, Adam W, Zhao CG, Bühler B, Schmid A, Bhalla G, Mironov O, Jones CJ, Tenn WJ, Nakamura S, ... Periana RA, et al. C-H Transformation at Unfunctionalized Alkanes Handbook of C-H Transformations: Applications in Organic Synthesis. 2: 497-651. DOI: 10.1002/9783527619450.ch9 |
0.772 |
|
| 2008 |
Rostovtsev VV, Snieckus V, Macklin T, Grushin VV, Ishiyama T, Miyaura N, Kakiuchi F, Dyker G, Kobayashi S, Bandini M, Melloni A, Piccinelli F, Reetz MT, Sommer K, Murai S, ... ... Periana RA, et al. C-H Transformation at Arenes Handbook of C-H Transformations: Applications in Organic Synthesis. 1: 99-276. DOI: 10.1002/9783527619450.ch5 |
0.775 |
|
| 2007 |
Gonzales JM, Distasio R, Periana RA, Goddard WA, Oxgaard J. Methylrhenium trioxide revisited: mechanisms for nonredox oxygen insertion in an M-CH3 bond. Journal of the American Chemical Society. 129: 15794-804. PMID 18052160 DOI: 10.1021/Ja0714742 |
0.551 |
|
| 2007 |
Oxgaard J, Tenn WJ, Nielsen RJ, Periana RA, Goddard WA. Mechanistic analysis of iridium heteroatom C-H activation: Evidence for an internal electrophilic substitution mechanism Organometallics. 26: 1565-1567. DOI: 10.1021/Om061189B |
0.79 |
|
| 2007 |
Young KJH, Mironov OA, Periana RA. Stoichiometric oxy functionalization and CH activation studies of cyclometalated iridium(III) 6-phenyl-2,2′-bipyridine hydrocarbyl complexes Organometallics. 26: 2137-2140. DOI: 10.1021/Om0611002 |
0.734 |
|
| 2007 |
Gonzales JM, Oxgaard J, Periana RA, Goddard WA. Methane activation with rhenium catalysts. 1. Bidentate oxygenated ligands Organometallics. 26: 1505-1511. DOI: 10.1021/Om0606901 |
0.49 |
|
| 2007 |
Periana RA, Meier SK, Young KJH, Tenn WJ, Oxgaard J, Goddard WA. Water and benzene H/D exchange by a cyclometallated Ir(III) bishydroxo pyridyl complex Acs National Meeting Book of Abstracts. |
0.795 |
|
| 2006 |
Conley BL, Ganesh SK, Gonzales JM, Tenn WJ, Young KJ, Oxgaard J, Goddard WA, Periana RA. Facile functionalization of a metal carbon bond by O-atom transfer. Journal of the American Chemical Society. 128: 9018-9. PMID 16834359 DOI: 10.1021/Ja062417W |
0.794 |
|
| 2006 |
Ziatdinov VR, Oxgaard J, Mironov OA, Young KJ, Goddard WA, Periana RA. Carboxylic solvents and O-donor ligand effects on CH activation by Pt(II). Journal of the American Chemical Society. 128: 7404-5. PMID 16756270 DOI: 10.1021/Ja060973K |
0.837 |
|
| 2006 |
Tenn WJ, Young KJH, Oxgaard J, Nielsen RJ, Goddard WA, Periana RA. Heterolytic CH activation and catalysis by an O-donor iridium-hydroxo complex Organometallics. 25: 5173-5175. DOI: 10.1021/Om060657E |
0.825 |
|
| 2006 |
Young KJH, Meier SK, Gonzales JM, Oxgaard J, Goddard WA, Periana RA. Heterolytic CH activation with a cyclometalated platinum(II) 6-phenyl-4,4′-di-tert-butyl-2,2-bipyridine complex Organometallics. 25: 4734-4737. DOI: 10.1021/Om060410H |
0.777 |
|
| 2006 |
Oxgaard J, Bhalla G, Periana RA, Goddard WA. Mechanistic investigation of indium-catalyzed hydrovinylation of olefins Organometallics. 25: 1618-1625. DOI: 10.1021/Om050890X |
0.741 |
|
| 2006 |
Conley BL, Tenn WJ, Young KJH, Ganesh SK, Meier SK, Ziatdinov VR, Mironov O, Oxgaard J, Gonzales J, Goddard WA, Periana RA. Design and study of homogeneous catalysts for the selective, low temperature oxidation of hydrocarbons Journal of Molecular Catalysis a: Chemical. 251: 8-23. DOI: 10.1016/J.Molcata.2006.02.035 |
0.802 |
|
| 2006 |
Conley BL, Tenn WJ, Young KJH, Ganesh S, Meier S, Ziatdinov V, Mironov O, Oxgaard J, Gonzales J, Goddard WA, Periana RA. Methane Functionalization Activation of Small Molecules: Organometallic and Bioinorganic Perspectives. 235-285. DOI: 10.1002/9783527609352.ch7 |
0.768 |
|
| 2005 |
Tenn WJ, Young KJ, Bhalla G, Oxgaard J, Goddard WA, Periana RA. CH activation with an O-donor iridium-methoxo complex. Journal of the American Chemical Society. 127: 14172-3. PMID 16218597 DOI: 10.1021/Ja051497L |
0.819 |
|
| 2005 |
Bhalla G, Liu XY, Oxgaard J, Goddard WA, Periana RA. Synthesis, structure, and reactivity of O-donor Ir(III) complexes: C-H activation studies with benzene. Journal of the American Chemical Society. 127: 11372-89. PMID 16089467 DOI: 10.1021/Ja051532O |
0.702 |
|
| 2005 |
Bhalla G, Periana RA. C-H activation of alkanes and arenes catalyzed by an O-donor bis(tropolonato)iridium(III) complex. Angewandte Chemie (International Ed. in English). 44: 1540-3. PMID 15674988 DOI: 10.1002/Anie.200462065 |
0.655 |
|
| 2005 |
Bhalla G, Oxgaard J, Goddard WA, Periana RA. Hydrovinylation of olefins catalyzed by an iridium complex via CH activation Organometallics. 24: 5499-5502. DOI: 10.1021/Om050614I |
0.725 |
|
| 2005 |
Bhalla G, Oxgaard J, Goddard WA, Periana RA. Anti-Markovnikov hydroarylation of unactivated olefins catalyzed by a bis-tropolonato iridium (III) organometallic complex Organometallics. 24: 3229-3232. DOI: 10.1021/Om0501733 |
0.69 |
|
| 2005 |
Periana RA, Mironov O, Taube D, Bhalla G, Jones CJ. Homogeneous, catalytic, oxidative coupling of methane to acetic acid in one step Topics in Catalysis. 32: 169-174. DOI: 10.1007/S11244-005-2887-4 |
0.752 |
|
| 2005 |
Ziatdinov VR, Mironov OA, Periana RA. Mechanism of benzene CH activation by BPYMPT complex Acs National Meeting Book of Abstracts. 229: INOR-649. |
0.811 |
|
| 2005 |
Ziatdinov VR, Young KJH, Periana RA. Synthesis and reactivity of novel platinum complexes Acs National Meeting Book of Abstracts. 229: INOR-815. |
0.796 |
|
| 2004 |
Oxgaard J, Periana RA, Goddard WA. Mechanistic analysis of hydroarylation catalysts. Journal of the American Chemical Society. 126: 11658-65. PMID 15366913 DOI: 10.1021/Ja048841J |
0.537 |
|
| 2004 |
Jones CJ, Taube D, Ziatdinov VR, Periana RA, Nielsen RJ, Oxgaard J, Goddard WA. Selective oxidation of methane to methanol catalyzed, with C-H activation, by homogeneous, cationic gold. Angewandte Chemie (International Ed. in English). 43: 4626-9. PMID 15316997 DOI: 10.1002/Anie.200461055 |
0.837 |
|
| 2004 |
Oxgaard J, Muller RP, Goddard WA, Periana RA. Mechanism of homogeneous Ir(III) catalyzed regioselective arylation of olefins. Journal of the American Chemical Society. 126: 352-63. PMID 14709102 DOI: 10.1021/Ja034126I |
0.561 |
|
| 2004 |
Liu XY, Tenn WJ, Bhalla G, Periana RA. Synthesis and structural characterization of novel organometallic, Rh(III), bis(acetylacetonate) complexes Organometallics. 23: 3584-3586. DOI: 10.1021/Om049741P |
0.832 |
|
| 2004 |
Xu X, Fu G, Goddard WA, Periana RA. Selective oxidation of CH4 to CH3OH using the Catalytica (bpym)PtCl2 catalyst: A theoretical study Studies in Surface Science and Catalysis. 147: 499-504. DOI: 10.1016/S0167-2991(04)80101-0 |
0.538 |
|
| 2004 |
Periana RA, Bhalla G, Tenn WJ, Young KJH, Liu XY, Mironov O, Jones CJ, Ziatdinov VR. Perspectives on some challenges and approaches for developing the next generation of selective, low temperature, oxidation catalysts for alkane hydroxylation based on the CH activation reaction Journal of Molecular Catalysis a: Chemical. 220: 7-25. DOI: 10.1016/J.Molcata.2004.05.036 |
0.82 |
|
| 2004 |
Periana RA. Chemistry and mechanism of new catalysts for the selective oxidation of hydrocarbons via the CH activation reaction Acs National Meeting Book of Abstracts. 228: INOR-410. |
0.358 |
|
| 2004 |
Periana RA, Mironov OA, Bhalla G, Jones CJ. Low-temperature, oxidative condensation of methane to acetic acid in one-step Acs National Meeting Book of Abstracts. 227: IEC-118. |
0.685 |
|
| 2003 |
Wong-Foy AG, Bhalla G, Liu XY, Periana RA. Alkane C-H activation and catalysis by an O-donor ligated iridium complex. Journal of the American Chemical Society. 125: 14292-3. PMID 14624574 DOI: 10.1021/Ja037849A |
0.679 |
|
| 2003 |
Periana RA, Mironov O, Taube D, Bhalla G, Jones CJ. Catalytic, oxidative condensation of CH4 to CH3COOH in one step via CH activation. Science (New York, N.Y.). 301: 814-8. PMID 12907796 DOI: 10.1126/Science.1086466 |
0.765 |
|
| 2003 |
Xu X, Kua J, Periana RA, Goddard WA. Structure, bonding, and stability of a catalytica platinum(II) catalyst: A computational study Organometallics. 22: 2057-2068. DOI: 10.1021/Om0202165 |
0.53 |
|
| 2002 |
Periana RA, Liu XY, Bhalla G. Novel bis-acac-O,O-Ir(III) catalyst for anti-Markovnikov, hydroarylation of olefins operates by arene CH activation. Chemical Communications (Cambridge, England). 3000-1. PMID 12536786 DOI: 10.1039/B208680H |
0.657 |
|
| 2002 |
Periana RA, Mironov O, Mirinov O, Taube DJ, Gamble S. High yield conversion of methane to methyl bisulfate catalyzed by iodine cations. Chemical Communications (Cambridge, England). 2376-7. PMID 12430448 DOI: 10.1039/B205366G |
0.623 |
|
| 2002 |
Kua J, Xu X, Periana RA, Goddard WA. Stability and thermodynamics of the PtCl2 type catalyst for activating methane to methanol: A computational study Organometallics. 21: 511-525. DOI: 10.1021/Om0101691 |
0.55 |
|
| 2002 |
Matsumoto T, Periana RA, Taube DJ, Yoshida H. Regioselective hydrophenylation of olefins catalyzed by an Ir(III) complex Journal of Molecular Catalysis a: Chemical. 180: 1-18. DOI: 10.1016/S1381-1169(01)00390-9 |
0.435 |
|
| 2002 |
Matsumoto T, Periana RA, Taube DJ, Yoshida H. Direct synthesis of styrene by rhodium-catalyzed oxidative arylation of ethylene with benzene Journal of Catalysis. 206: 272-280. DOI: 10.1006/Jcat.2001.3471 |
0.523 |
|
| 2001 |
Arakawa H, Aresta M, Armor JN, Barteau MA, Beckman EJ, Bell AT, Bercaw JE, Creutz C, Dinjus E, Dixon DA, Domen K, DuBois DL, Eckert J, Fujita E, Gibson DH, ... ... Periana R, et al. Catalysis research of relevance to carbon management: progress, challenges, and opportunities. Chemical Reviews. 101: 953-96. PMID 11709862 DOI: 10.1021/Cr000018S |
0.461 |
|
| 2000 |
Matsumoto T, Taube DJ, Periana RA, Taube H, Yoshida H. Anti-Markovnikov olefin arylation catalyzed by an iridium complex [15] Journal of the American Chemical Society. 122: 7414-7415. DOI: 10.1021/Ja0009830 |
0.528 |
|
| 1998 |
Periana RA, Taube DJ, Gamble S, Taube H, Satoh T, Fujii H. Platinum catalysts for the high-yield oxidation of methane to a methanol derivative Science (New York, N.Y.). 280: 560-4. PMID 9554841 DOI: 10.1126/Science.280.5363.560 |
0.611 |
|
| 1997 |
Periana RA. A novel, high-yield system for the oxidation of methane to methanol Advances in Chemistry Series. 253: 61-78. DOI: 10.1016/S0167-2991(08)63925-7 |
0.46 |
|
| 1995 |
Horsley JA, Vanderveken DJ, Periana RA. Computational study of the highly efficient conversion of methane to methanol with mercury (II) catalysts Catalysis Today. 23: 333-339. DOI: 10.1016/0920-5861(94)00146-S |
0.385 |
|
| 1993 |
Periana RA, Taube DJ, Evitt ER, Löffler DG, Wentrcek PR, Voss G, Masuda T. A mercury-catalyzed, high-yield system for the oxidation of methane to methanol. Science (New York, N.Y.). 259: 340-3. PMID 17832346 DOI: 10.1126/Science.259.5093.340 |
0.456 |
|
| 1992 |
Dygos JH, Yonan EE, Scaros MG, Goodmonson OJ, Getman DP, Periana RA, Beck GR. A convenient asymmetric synthesis of the unnatural amino acid 2,6-dimethyl-L-tyrosine Synthesis. 741-743. DOI: 10.1055/S-1992-26212 |
0.324 |
|
| 1987 |
PERIANA RA, BERGMAN RG. ChemInform Abstract: C-C Activation of Organic Small Ring Compounds by Rearrangement of Cycloalkylhydridorhodium Complexes to Rhodacycloalkanes. Synthesis of Metallacyclobutanes, Including One with a Tertiary M-C Bond, by Nucleophilic Addition to π-Allyl Cheminform. 18. DOI: 10.1002/chin.198713311 |
0.4 |
|
| 1987 |
PERIANA RA, BERGMAN RG. ChemInform Abstract: Isomerization of the Hydridoalkylrhodium Complexes Formed on Oxidative Addition of Rhodium to Alkane C-H Bonds. Evidence for the Intermediacy of η2-Alkane Complexes. Cheminform. 18. DOI: 10.1002/chin.198713310 |
0.481 |
|
| 1987 |
PERIANA RA, BERGMAN RG. ChemInform Abstract: Isomerization of the Hydridoalkylrhodium Complexes Formed on Oxidative Addition of Rhodium to Alkane C-H Bonds. Evidence for the Intermediacy of η2-Alkane Complexes. Cheminform. 18. DOI: 10.1002/chin.198713310 |
0.481 |
|
| 1986 |
Periana RA, Bergman RG. Carbon-carbon activation of organic small ring compounds by arrangement of cycloalkylhydridorhodium complexes to rhodacycloalkanes. Synthesis of metallacyclobutanes, including one with a tertiary metal-carbon bond, by nucleophilic addition to .pi.-allyl complexes Journal of the American Chemical Society. 108: 7346-7355. DOI: 10.1021/Ja00283A033 |
0.401 |
|
| 1986 |
Periana RA, Bergman RG. Carbon-carbon activation of organic small ring compounds by arrangement of cycloalkylhydridorhodium complexes to rhodacycloalkanes. Synthesis of metallacyclobutanes, including one with a tertiary metal-carbon bond, by nucleophilic addition to .pi.-allyl complexes Journal of the American Chemical Society. 108: 7346-7355. DOI: 10.1021/Ja00283A033 |
0.401 |
|
| 1986 |
Periana RA, Bergman RG. Carbon-carbon activation of organic small ring compounds by arrangement of cycloalkylhydridorhodium complexes to rhodacycloalkanes. Synthesis of metallacyclobutanes, including one with a tertiary metal-carbon bond, by nucleophilic addition to .pi.-allyl complexes Journal of the American Chemical Society. 108: 7346-7355. DOI: 10.1021/Ja00283A033 |
0.401 |
|
| 1986 |
Periana RA, Bergman RG. Carbon-carbon activation of organic small ring compounds by arrangement of cycloalkylhydridorhodium complexes to rhodacycloalkanes. Synthesis of metallacyclobutanes, including one with a tertiary metal-carbon bond, by nucleophilic addition to .pi.-allyl complexes Journal of the American Chemical Society. 108: 7346-7355. DOI: 10.1021/Ja00283A033 |
0.401 |
|
| 1986 |
Periana RA, Bergman RG. Carbon-carbon activation of organic small ring compounds by arrangement of cycloalkylhydridorhodium complexes to rhodacycloalkanes. Synthesis of metallacyclobutanes, including one with a tertiary metal-carbon bond, by nucleophilic addition to .pi.-allyl complexes Journal of the American Chemical Society. 108: 7346-7355. DOI: 10.1021/Ja00283A033 |
0.401 |
|
| 1986 |
Periana RA, Bergman RG. Carbon-carbon activation of organic small ring compounds by arrangement of cycloalkylhydridorhodium complexes to rhodacycloalkanes. Synthesis of metallacyclobutanes, including one with a tertiary metal-carbon bond, by nucleophilic addition to .pi.-allyl complexes Journal of the American Chemical Society. 108: 7346-7355. DOI: 10.1021/Ja00283A033 |
0.401 |
|
| 1986 |
Periana RA, Bergman RG. Carbon-carbon activation of organic small ring compounds by arrangement of cycloalkylhydridorhodium complexes to rhodacycloalkanes. Synthesis of metallacyclobutanes, including one with a tertiary metal-carbon bond, by nucleophilic addition to .pi.-allyl complexes Journal of the American Chemical Society. 108: 7346-7355. DOI: 10.1021/Ja00283A033 |
0.401 |
|
| 1986 |
Periana RA, Bergman RG. Carbon-carbon activation of organic small ring compounds by arrangement of cycloalkylhydridorhodium complexes to rhodacycloalkanes. Synthesis of metallacyclobutanes, including one with a tertiary metal-carbon bond, by nucleophilic addition to .pi.-allyl complexes Journal of the American Chemical Society. 108: 7346-7355. DOI: 10.1021/Ja00283A033 |
0.401 |
|
| 1986 |
Periana RA, Bergman RG. Carbon-carbon activation of organic small ring compounds by arrangement of cycloalkylhydridorhodium complexes to rhodacycloalkanes. Synthesis of metallacyclobutanes, including one with a tertiary metal-carbon bond, by nucleophilic addition to .pi.-allyl complexes Journal of the American Chemical Society. 108: 7346-7355. DOI: 10.1021/Ja00283A033 |
0.401 |
|
| 1986 |
Periana RA, Bergman RG. Carbon-carbon activation of organic small ring compounds by arrangement of cycloalkylhydridorhodium complexes to rhodacycloalkanes. Synthesis of metallacyclobutanes, including one with a tertiary metal-carbon bond, by nucleophilic addition to .pi.-allyl complexes Journal of the American Chemical Society. 108: 7346-7355. DOI: 10.1021/Ja00283A033 |
0.401 |
|
| 1986 |
Periana RA, Bergman RG. Carbon-carbon activation of organic small ring compounds by arrangement of cycloalkylhydridorhodium complexes to rhodacycloalkanes. Synthesis of metallacyclobutanes, including one with a tertiary metal-carbon bond, by nucleophilic addition to .pi.-allyl complexes Journal of the American Chemical Society. 108: 7346-7355. DOI: 10.1021/Ja00283A033 |
0.401 |
|
| 1986 |
Periana RA, Bergman RG. Isomerization of the hydridoalkylrhodium complexes formed on oxidative addition of rhodium to alkane carbon-hydrogen bonds. Evidence for the intermediacy of .eta.2-alkane complexes Journal of the American Chemical Society. 108: 7332-7346. DOI: 10.1021/Ja00283A032 |
0.443 |
|
| 1986 |
Periana RA, Bergman RG. Isomerization of the hydridoalkylrhodium complexes formed on oxidative addition of rhodium to alkane carbon-hydrogen bonds. Evidence for the intermediacy of .eta.2-alkane complexes Journal of the American Chemical Society. 108: 7332-7346. DOI: 10.1021/Ja00283A032 |
0.443 |
|
| 1986 |
Periana RA, Bergman RG. Isomerization of the hydridoalkylrhodium complexes formed on oxidative addition of rhodium to alkane C-H bonds. Evidence for the intermediacy of η2-alkane complexes Journal of the American Chemical Society. 108: 7332-7346. |
0.309 |
|
| 1985 |
PERIANA RA, BERGMAN RG. ChemInform Abstract: RAPID INTRAMOLECULAR REARRANGEMENT OF A HYDRIDO(CYCLOPROPYL)RHODIUM COMPLEX TO A RHODACYCLOBUTANE. INDEPENDENT SYNTHESIS OF THE METALLACYCLE BY ADDITION OF HYDRIDE TO THE CENTRAL CARBON ATOM OF A CATIONIC RHODIUM Π-ALLYL COMPLEX Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198511293 |
0.416 |
|
| 1985 |
PERIANA RA, BERGMAN RG. ChemInform Abstract: RAPID INTRAMOLECULAR REARRANGEMENT OF A HYDRIDO(CYCLOPROPYL)RHODIUM COMPLEX TO A RHODACYCLOBUTANE. INDEPENDENT SYNTHESIS OF THE METALLACYCLE BY ADDITION OF HYDRIDE TO THE CENTRAL CARBON ATOM OF A CATIONIC RHODIUM Π-ALLYL COMPLEX Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198511293 |
0.416 |
|
| 1985 |
PERIANA RA, BERGMAN RG. ChemInform Abstract: RAPID INTRAMOLECULAR REARRANGEMENT OF A HYDRIDO(CYCLOPROPYL)RHODIUM COMPLEX TO A RHODACYCLOBUTANE. INDEPENDENT SYNTHESIS OF THE METALLACYCLE BY ADDITION OF HYDRIDE TO THE CENTRAL CARBON ATOM OF A CATIONIC RHODIUM Π-ALLYL COMPLEX Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198511293 |
0.416 |
|
| 1985 |
PERIANA RA, BERGMAN RG. ChemInform Abstract: RAPID INTRAMOLECULAR REARRANGEMENT OF A HYDRIDO(CYCLOPROPYL)RHODIUM COMPLEX TO A RHODACYCLOBUTANE. INDEPENDENT SYNTHESIS OF THE METALLACYCLE BY ADDITION OF HYDRIDE TO THE CENTRAL CARBON ATOM OF A CATIONIC RHODIUM Π-ALLYL COMPLEX Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198511293 |
0.416 |
|
| 1985 |
PERIANA RA, BERGMAN RG. ChemInform Abstract: RAPID INTRAMOLECULAR REARRANGEMENT OF A HYDRIDO(CYCLOPROPYL)RHODIUM COMPLEX TO A RHODACYCLOBUTANE. INDEPENDENT SYNTHESIS OF THE METALLACYCLE BY ADDITION OF HYDRIDE TO THE CENTRAL CARBON ATOM OF A CATIONIC RHODIUM Π-ALLYL COMPLEX Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198511293 |
0.416 |
|
| 1985 |
PERIANA RA, BERGMAN RG. ChemInform Abstract: RAPID INTRAMOLECULAR REARRANGEMENT OF A HYDRIDO(CYCLOPROPYL)RHODIUM COMPLEX TO A RHODACYCLOBUTANE. INDEPENDENT SYNTHESIS OF THE METALLACYCLE BY ADDITION OF HYDRIDE TO THE CENTRAL CARBON ATOM OF A CATIONIC RHODIUM Π-ALLYL COMPLEX Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198511293 |
0.416 |
|
| 1984 |
Janowicz AH, Periana RA, Buchanan JM, Kovac CA, Stryker JM, Wax MJ, Bergman RG. Oxidative addition of soluble iridium and rhodium complexes to carbon-hydrogen bonds in methane and higher alkanes (1) Pure and Applied Chemistry. 56: 13-23. DOI: 10.1351/Pac198456010013 |
0.689 |
|
| 1984 |
Janowicz AH, Periana RA, Buchanan JM, Kovac CA, Stryker JM, Wax MJ, Bergman RG. Oxidative addition of soluble iridium and rhodium complexes to carbon-hydrogen bonds in methane and higher alkanes (1) Pure and Applied Chemistry. 56: 13-23. DOI: 10.1351/Pac198456010013 |
0.689 |
|
| 1984 |
Janowicz AH, Periana RA, Buchanan JM, Kovac CA, Stryker JM, Wax MJ, Bergman RG. Oxidative addition of soluble iridium and rhodium complexes to carbon-hydrogen bonds in methane and higher alkanes (1) Pure and Applied Chemistry. 56: 13-23. DOI: 10.1351/Pac198456010013 |
0.689 |
|
| 1984 |
Janowicz AH, Periana RA, Buchanan JM, Kovac CA, Stryker JM, Wax MJ, Bergman RG. Oxidative addition of soluble iridium and rhodium complexes to carbon-hydrogen bonds in methane and higher alkanes (1) Pure and Applied Chemistry. 56: 13-23. DOI: 10.1351/Pac198456010013 |
0.689 |
|
| 1984 |
Janowicz AH, Periana RA, Buchanan JM, Kovac CA, Stryker JM, Wax MJ, Bergman RG. Oxidative addition of soluble iridium and rhodium complexes to carbon-hydrogen bonds in methane and higher alkanes (1) Pure and Applied Chemistry. 56: 13-23. DOI: 10.1351/Pac198456010013 |
0.689 |
|
| 1984 |
Janowicz AH, Periana RA, Buchanan JM, Kovac CA, Stryker JM, Wax MJ, Bergman RG. Oxidative addition of soluble iridium and rhodium complexes to carbon-hydrogen bonds in methane and higher alkanes (1) Pure and Applied Chemistry. 56: 13-23. DOI: 10.1351/Pac198456010013 |
0.689 |
|
| 1984 |
Janowicz AH, Periana RA, Buchanan JM, Kovac CA, Stryker JM, Wax MJ, Bergman RG. Oxidative addition of soluble iridium and rhodium complexes to carbon-hydrogen bonds in methane and higher alkanes (1) Pure and Applied Chemistry. 56: 13-23. DOI: 10.1351/Pac198456010013 |
0.689 |
|
| 1984 |
Janowicz AH, Periana RA, Buchanan JM, Kovac CA, Stryker JM, Wax MJ, Bergman RG. Oxidative addition of soluble iridium and rhodium complexes to carbon-hydrogen bonds in methane and higher alkanes (1) Pure and Applied Chemistry. 56: 13-23. DOI: 10.1351/Pac198456010013 |
0.689 |
|
| 1984 |
Janowicz AH, Periana RA, Buchanan JM, Kovac CA, Stryker JM, Wax MJ, Bergman RG. Oxidative addition of soluble iridium and rhodium complexes to carbon-hydrogen bonds in methane and higher alkanes (1) Pure and Applied Chemistry. 56: 13-23. DOI: 10.1351/Pac198456010013 |
0.689 |
|
| 1984 |
Janowicz AH, Periana RA, Buchanan JM, Kovac CA, Stryker JM, Wax MJ, Bergman RG. Oxidative addition of soluble iridium and rhodium complexes to carbon-hydrogen bonds in methane and higher alkanes (1) Pure and Applied Chemistry. 56: 13-23. DOI: 10.1351/Pac198456010013 |
0.689 |
|
| 1984 |
Janowicz AH, Periana RA, Buchanan JM, Kovac CA, Stryker JM, Wax MJ, Bergman RG. Oxidative addition of soluble iridium and rhodium complexes to carbon-hydrogen bonds in methane and higher alkanes (1) Pure and Applied Chemistry. 56: 13-23. DOI: 10.1351/Pac198456010013 |
0.689 |
|
| 1984 |
Janowicz AH, Periana RA, Buchanan JM, Kovac CA, Stryker JM, Wax MJ, Bergman RG. Oxidative addition of soluble iridium and rhodium complexes to carbon-hydrogen bonds in methane and higher alkanes (1) Pure and Applied Chemistry. 56: 13-23. DOI: 10.1351/Pac198456010013 |
0.689 |
|
| 1984 |
Periana RA, Bergman RG. Oxidative addition of rhodium to alkane carbon-hydrogen bonds: enhancement in selectivity and alkyl group functionalization Organometallics. 3: 508-510. DOI: 10.1021/Om00081A038 |
0.428 |
|
| 1984 |
Periana RA, Bergman RG. Oxidative addition of rhodium to alkane carbon-hydrogen bonds: enhancement in selectivity and alkyl group functionalization Organometallics. 3: 508-510. DOI: 10.1021/Om00081A038 |
0.428 |
|
| 1984 |
Periana RA, Bergman RG. Rapid intramolecular rearrangement of a hydrido(cyclopropyl)rhodium complex to a rhodacyclobutane. Independent synthesis of the metallacycle by addition of hydride to the central carbon atom of a cationic rhodium .pi.-allyl complex Journal of the American Chemical Society. 106: 7272-7273. DOI: 10.1021/Ja00335A084 |
0.414 |
|
| 1984 |
Periana RA, Bergman RG. Rapid intramolecular rearrangement of a hydrido(cyclopropyl)rhodium complex to a rhodacyclobutane. Independent synthesis of the metallacycle by addition of hydride to the central carbon atom of a cationic rhodium .pi.-allyl complex Journal of the American Chemical Society. 106: 7272-7273. DOI: 10.1021/Ja00335A084 |
0.414 |
|
| 1984 |
Periana RA, Bergman RG. Rapid intramolecular rearrangement of a hydrido(cyclopropyl)rhodium complex to a rhodacyclobutane. Independent synthesis of the metallacycle by addition of hydride to the central carbon atom of a cationic rhodium .pi.-allyl complex Journal of the American Chemical Society. 106: 7272-7273. DOI: 10.1021/Ja00335A084 |
0.414 |
|
| 1984 |
Periana RA, Bergman RG. Rapid intramolecular rearrangement of a hydrido(cyclopropyl)rhodium complex to a rhodacyclobutane. Independent synthesis of the metallacycle by addition of hydride to the central carbon atom of a cationic rhodium .pi.-allyl complex Journal of the American Chemical Society. 106: 7272-7273. DOI: 10.1021/Ja00335A084 |
0.414 |
|
| 1984 |
Periana RA, Bergman RG. Rapid intramolecular rearrangement of a hydrido(cyclopropyl)rhodium complex to a rhodacyclobutane. Independent synthesis of the metallacycle by addition of hydride to the central carbon atom of a cationic rhodium .pi.-allyl complex Journal of the American Chemical Society. 106: 7272-7273. DOI: 10.1021/Ja00335A084 |
0.414 |
|
| 1984 |
Periana RA, Bergman RG. Rapid intramolecular rearrangement of a hydrido(cyclopropyl)rhodium complex to a rhodacyclobutane. Independent synthesis of the metallacycle by addition of hydride to the central carbon atom of a cationic rhodium .pi.-allyl complex Journal of the American Chemical Society. 106: 7272-7273. DOI: 10.1021/Ja00335A084 |
0.414 |
|
| 1984 |
Periana RA, Bergman RG. Rapid intramolecular rearrangement of a hydrido(cyclopropyl)rhodium complex to a rhodacyclobutane. Independent synthesis of the metallacycle by addition of hydride to the central carbon atom of a cationic rhodium .pi.-allyl complex Journal of the American Chemical Society. 106: 7272-7273. DOI: 10.1021/Ja00335A084 |
0.414 |
|
| 1984 |
Periana RA, Bergman RG. Rapid intramolecular rearrangement of a hydrido(cyclopropyl)rhodium complex to a rhodacyclobutane. Independent synthesis of the metallacycle by addition of hydride to the central carbon atom of a cationic rhodium .pi.-allyl complex Journal of the American Chemical Society. 106: 7272-7273. DOI: 10.1021/Ja00335A084 |
0.414 |
|
| 1984 |
Periana RA, Bergman RG. Rapid intramolecular rearrangement of a hydrido(cyclopropyl)rhodium complex to a rhodacyclobutane. Independent synthesis of the metallacycle by addition of hydride to the central carbon atom of a cationic rhodium .pi.-allyl complex Journal of the American Chemical Society. 106: 7272-7273. DOI: 10.1021/Ja00335A084 |
0.414 |
|
| 1984 |
Periana RA, Bergman RG. Rapid intramolecular rearrangement of a hydrido(cyclopropyl)rhodium complex to a rhodacyclobutane. Independent synthesis of the metallacycle by addition of hydride to the central carbon atom of a cationic rhodium .pi.-allyl complex Journal of the American Chemical Society. 106: 7272-7273. DOI: 10.1021/Ja00335A084 |
0.414 |
|
| 1984 |
Periana RA, Bergman RG. Rapid intramolecular rearrangement of a hydrido(cyclopropyl)rhodium complex to a rhodacyclobutane. Independent synthesis of the metallacycle by addition of hydride to the central carbon atom of a cationic rhodium .pi.-allyl complex Journal of the American Chemical Society. 106: 7272-7273. DOI: 10.1021/Ja00335A084 |
0.414 |
|
| 1984 |
Periana RA, Bergman RG. Rapid intramolecular rearrangement of a hydrido(cyclopropyl)rhodium complex to a rhodacyclobutane. Independent synthesis of the metallacycle by addition of hydride to the central carbon atom of a cationic rhodium .pi.-allyl complex Journal of the American Chemical Society. 106: 7272-7273. DOI: 10.1021/Ja00335A084 |
0.414 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2005 |
Periana RA. Transition Metal Arene π-Complexes in Organic Synthesis and Catalysis. Topics in Organometallic Chemistry, 7 Edited by E. Peter Kündig (University of Geneva). Springer-Verlag: Berlin, Heidelberg, New York. 2004. viii + 232 pp. $269.00. ISBN 3-540-01604-X. Journal of the American Chemical Society. 127: 1589-1589. DOI: 10.1021/Ja040984I |
0.296 |
|
| 1984 |
Periana RA, Bergman RG. Oxidative addition of rhodium to alkane C-H bonds: Enhancement in selectivity and alkyl group functionalization Organometallics. 3: 508-510. |
0.296 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
|
| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
0.293 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
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| 2018 |
King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
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King CR, Rollins N, Holdaway A, Konnick MM, Periana RA, Ess DH. Electrophilic Impact of High-Oxidation State Main-Group Metal and Ligands on Alkane C–H Activation and Functionalization Reactions Organometallics. 37: 3045-3054. DOI: 10.1021/acs.organomet.8b00418 |
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| 1980 |
Periana RA, Motiu-DeGrood R, Chiang Y, Hupe DJ. Does substrate rather than protein provide the catalyst for .alpha.-proton abstraction in aldolase? Journal of the American Chemical Society. 102: 3923-3927. DOI: 10.1021/Ja00531A040 |
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| 2010 |
Song G, Su Y, Periana RA, Crabtree RH, Han K, Zhang H, Li X. Anion-exchange-triggered 1,3-shift of an NH proton to iridium in protic n-heterocyclic carbenes: hydrogen-bonding and ion-pairing effects. Angewandte Chemie (International Ed. in English). 49: 912-7. PMID 20039244 DOI: 10.1002/Anie.200905691 |
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| 2011 |
Goddard WA, Sha Y, Meyer TJ, Periana RA. Progress in catalytic processes for fuel cells Acs National Meeting Book of Abstracts. |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
|
| 2020 |
Gunsalus NJ, Koppaka A, Hashiguchi BG, Konnick MM, Park SH, Ess DH, Periana RA. SN2 and E2 Branching of Main-Group-Metal Alkyl Intermediates in Alkane CH Oxidation: Mechanistic Investigation Using Isotopically Labeled Main-Group-Metal Alkyls Organometallics. 39: 1907-1916. DOI: 10.1021/acs.organomet.0c00120 |
0.27 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
|
| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
0.248 |
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| 2016 |
Fuller JT, Butler S, Devarajan D, Jacobs A, Hashiguchi BG, Konnick MM, Goddard WA, Gonzales J, Periana RA, Ess DH. Catalytic Mechanism and Efficiency of Methane Oxidation by Hg(II) in Sulfuric Acid and Comparison to Radical Initiated Conditions Acs Catalysis. 6: 4312-4322. DOI: 10.1021/acscatal.6b00226 |
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| 2007 |
Periana RA. Breakthroughs in oxidizing CH4 and prospects for the 21st century Acs National Meeting Book of Abstracts. |
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| 1986 |
Periana RA, Bergman RG. C-C activation of organic small ring compounds by rearrangement of cycloalkylhydridorhodium complexes to rhodacycloalkanes. Synthesis of metallacyclobutanes, including one with a tertiary M-C bond, by nucleophilic addition to π-allyl complexes Journal of the American Chemical Society. 108: 7346-7355. |
0.222 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
|
| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 2019 |
Gunsalus NJ, Park SH, Hashiguchi BG, Koppaka A, Smith SJ, Ess DH, Periana RA. Selective N Functionalization of Methane and Ethane to Aminated Derivatives by Main-Group-Directed C–H Activation Organometallics. 38: 2319-2322. DOI: 10.1021/acs.organomet.9b00246 |
0.221 |
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| 1984 |
Periana RA, Bergman RG. Rapid intramolecular rearrangement of a hydridocyclopropylrhodium complex to a rhodacyclobutane. Independent synthesis of the metallacycle by addition of hydride to the central carbon atom of a cationic rhodium π-allyl complex Journal of the American Chemical Society. 106: 7272-7273. |
0.218 |
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| 1994 |
Periana RA, Taube DJ, Evitt ER, Löffler DG, Wentrcek PR, Voss G, Masuda T. A Novel, High Yield System for the Oxidation of Methane to Methanol Studies in Surface Science and Catalysis. 81: 533-544. DOI: 10.1016/S0167-2991(08)63925-7 |
0.211 |
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| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
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| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
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| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
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| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
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| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
|
| 2016 |
King CR, Gustafson SJ, Black BR, Butler SK, Konnick MM, Periana RA, Hashiguchi BM, Ess DH. Arene C–H Functionalization by p-Block Metal Tl(III) Occurs at the Borderline of C–H Activation and Electron Transfer Organometallics. 36: 109-113. DOI: 10.1021/acs.organomet.6b00475 |
0.208 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2008 |
Bhalla G, Mironov O, Jones CJ, Tenn WJI, Nakamura S, Periana RA. ChemInform Abstract: Transition Metal-Catalyzed Oxidation of Alkanes Cheminform. 39. DOI: 10.1002/chin.200809265 |
0.206 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
|
| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
0.175 |
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| 2018 |
Gustafson SJ, Konnick MM, Periana RA, Ess DH. Mechanisms and Reactivity of Tl(III) Main-Group-Metal–Alkyl Functionalization in Water Organometallics. 37: 2723-2731. DOI: 10.1021/acs.organomet.8b00371 |
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Periana RA, Motiu-DeGrood R, Chiang Y, Hupe DJ. Does substrate rather than protein provide the catalyst for α-proton abstraction in aldolase? Journal of the American Chemical Society. 102: 3923-3927. |
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| 2005 |
Periana RA. Transition Metal Arene π-Complexes in Organic Synthesis and Catalysis. Topics in Organometallic Chemistry, 7 Edited by E. Peter Kündig (University of Geneva). Springer-Verlag: Berlin, Heidelberg, New York. 2004. viii + 232 pp. $269.00. ISBN 3-540-01604-X. Journal of the American Chemical Society. 127: 1589-1589. DOI: 10.1021/ja040984i |
0.156 |
|
| 2005 |
Periana RA. Transition Metal Arene π-Complexes in Organic Synthesis and Catalysis. Topics in Organometallic Chemistry, 7 Edited by E. Peter Kündig (University of Geneva). Springer-Verlag: Berlin, Heidelberg, New York. 2004. viii + 232 pp. $269.00. ISBN 3-540-01604-X. Journal of the American Chemical Society. 127: 1589-1589. DOI: 10.1021/ja040984i |
0.156 |
|
| 2005 |
Periana RA. Transition Metal Arene π-Complexes in Organic Synthesis and Catalysis. Topics in Organometallic Chemistry, 7 Edited by E. Peter Kündig (University of Geneva). Springer-Verlag: Berlin, Heidelberg, New York. 2004. viii + 232 pp. $269.00. ISBN 3-540-01604-X. Journal of the American Chemical Society. 127: 1589-1589. DOI: 10.1021/ja040984i |
0.156 |
|
| 2005 |
Periana RA. Transition Metal Arene π-Complexes in Organic Synthesis and Catalysis. Topics in Organometallic Chemistry, 7 Edited by E. Peter Kündig (University of Geneva). Springer-Verlag: Berlin, Heidelberg, New York. 2004. viii + 232 pp. $269.00. ISBN 3-540-01604-X. Journal of the American Chemical Society. 127: 1589-1589. DOI: 10.1021/ja040984i |
0.156 |
|
| 2005 |
Periana RA. Transition Metal Arene π-Complexes in Organic Synthesis and Catalysis. Topics in Organometallic Chemistry, 7 Edited by E. Peter Kündig (University of Geneva). Springer-Verlag: Berlin, Heidelberg, New York. 2004. viii + 232 pp. $269.00. ISBN 3-540-01604-X. Journal of the American Chemical Society. 127: 1589-1589. DOI: 10.1021/ja040984i |
0.156 |
|
| 2005 |
Periana RA. Transition Metal Arene π-Complexes in Organic Synthesis and Catalysis. Topics in Organometallic Chemistry, 7 Edited by E. Peter Kündig (University of Geneva). Springer-Verlag: Berlin, Heidelberg, New York. 2004. viii + 232 pp. $269.00. ISBN 3-540-01604-X. Journal of the American Chemical Society. 127: 1589-1589. DOI: 10.1021/ja040984i |
0.156 |
|
| 2005 |
Periana RA. Transition Metal Arene π-Complexes in Organic Synthesis and Catalysis. Topics in Organometallic Chemistry, 7 Edited by E. Peter Kündig (University of Geneva). Springer-Verlag: Berlin, Heidelberg, New York. 2004. viii + 232 pp. $269.00. ISBN 3-540-01604-X. Journal of the American Chemical Society. 127: 1589-1589. DOI: 10.1021/ja040984i |
0.156 |
|
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