Year |
Citation |
Score |
2023 |
Zhang L, Lu Z, Rander AR, Williams TJ. An ambient pressure, direct hydrogenation of ketones. Chemical Communications (Cambridge, England). 59: 8107-8110. PMID 37294535 DOI: 10.1039/d3cc01014g |
0.543 |
|
2023 |
Nalikezhathu A, Tam A, Cherepakhin V, Do VK, Williams TJ. Synthesis of 1,4-Diazacycles by Hydrogen Borrowing. Organic Letters. PMID 36867725 DOI: 10.1021/acs.orglett.3c00468 |
0.381 |
|
2022 |
Do VK, Vargas NA, Chavez AJ, Zhang L, Cherepakhin V, Lu Z, Currier RP, Dub PA, Gordon JC, Williams TJ. Pressurized Formic Acid Dehydrogenation: An Entropic Spring Replaces Hydrogen Compression Cost. Catalysis Science & Technology. 12: 7182-7189. PMID 37192930 DOI: 10.1039/d2cy00676f |
0.542 |
|
2020 |
Cherepakhin V, Hellman A, Lan Z, Mallikarjun Sharada S, Williams TJ. Heterobimetallic complexes of IrM (M = Fe, Co, and Ni) core and bridging 2-(diphenylphosphino)pyridine: electronic structure and electrochemical behavior. Dalton Transactions (Cambridge, England : 2003). 49: 10509-10515. PMID 32748911 DOI: 10.1039/D0Dt01801E |
0.357 |
|
2020 |
Nalikezhathu A, Cherepakhin V, Williams TJ. Ruthenium Catalyzed Tandem Pictet-Spengler Reaction. Organic Letters. PMID 32558575 DOI: 10.1021/Acs.Orglett.0C01485 |
0.356 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2020 |
Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508 |
0.303 |
|
2019 |
Cherepakhin V, Williams TJ. Catalyst Evolution in Ruthenium-Catalyzed Coupling of Amines and Alcohols Acs Catalysis. 10: 56-65. DOI: 10.1021/Acscatal.9B03679 |
0.369 |
|
2019 |
Demianets I, Hunt JR, Dawlaty JM, Williams TJ. Optical pKa Control in a Bifunctional Iridium Complex Organometallics. 38: 200-204. DOI: 10.1021/Acs.Organomet.8B00778 |
0.429 |
|
2018 |
Lu Z, Cherepakhin V, Kapenstein T, Williams TJ. Upgrading Biodiesel from Vegetable Oils by Hydrogen Transfer to its Fatty Esters. Acs Sustainable Chemistry & Engineering. 6: 5749-5753. PMID 30319930 DOI: 10.1021/Acssuschemeng.8B00653 |
0.589 |
|
2018 |
Cherepakhin V, Williams TJ. Iridium Catalysts for Acceptorless Dehydrogenation of Alcohols to Carboxylic Acids: Scope and Mechanism. Acs Catalysis. 8: 3754-3763. PMID 30288338 DOI: 10.1021/Acscatal.8B00105 |
0.409 |
|
2018 |
Navarro CA, Kedzie EA, Ma Y, Michael KH, Nutt SR, Williams TJ. Mechanism and Catalysis of Oxidative Degradation of Fiber-Reinforced Epoxy Composites. Topics in Catalysis. 61: 704-709. PMID 30288016 DOI: 10.1007/S11244-018-0917-2 |
0.31 |
|
2018 |
Lauridsen PJ, Lu Z, Celaje JJA, Kedzie EA, Williams TJ. Conformational twisting of a formate-bridged diiridium complex enables catalytic formic acid dehydrogenation. Dalton Transactions (Cambridge, England : 2003). PMID 30206593 DOI: 10.1039/C8Dt03268H |
0.784 |
|
2018 |
Lu Z, Cherepakhin V, Demianets I, Lauridsen PJ, Williams TJ. Iridium-based hydride transfer catalysts: from hydrogen storage to fine chemicals. Chemical Communications (Cambridge, England). PMID 29888372 DOI: 10.1039/C8Cc03412E |
0.622 |
|
2017 |
Lee H, Feakins SJ, Lu Z, Schimmelmann A, Sessions AL, Tierney JE, Williams TJ. Comparison of three methods for the methylation of aliphatic and aromatic compounds. Rapid Communications in Mass Spectrometry : Rcm. PMID 28763166 DOI: 10.1002/Rcm.7947 |
0.527 |
|
2017 |
Celaje JJA, Zhang X, Zhang F, Kam L, Herron JR, Williams TJ. A Base and Solvent-Free Ruthenium-Catalyzed Alkylation of Amines Acs Catalysis. 7: 1136-1142. DOI: 10.1021/Acscatal.6B03088 |
0.836 |
|
2016 |
Zhang X, Kam L, Trerise R, Williams TJ. Ruthenium-Catalyzed Ammonia Borane Dehydrogenation: Mechanism and Utility. Accounts of Chemical Research. PMID 28032510 DOI: 10.1021/Acs.Accounts.6B00482 |
0.455 |
|
2016 |
Celaje JJ, Lu Z, Kedzie EA, Terrile NJ, Lo JN, Williams TJ. A prolific catalyst for dehydrogenation of neat formic acid. Nature Communications. 7: 11308. PMID 27076111 DOI: 10.1038/Ncomms11308 |
0.8 |
|
2016 |
Zhang X, Kam L, Williams TJ. Dehydrogenation of ammonia borane through the third equivalent of hydrogen. Dalton Transactions (Cambridge, England : 2003). PMID 27052687 DOI: 10.1039/C6Dt00604C |
0.346 |
|
2016 |
Lu Z, Williams TJ. Di(carbene)-Supported Nickel Systems for CO2 Reduction under Ambient Conditions Acs Catalysis. 6: 6670-6673. DOI: 10.1021/Acscatal.6B02101 |
0.634 |
|
2016 |
Lu Z, Demianets I, Hamze R, Terrile NJ, Williams TJ. A Prolific Catalyst for Selective Conversion of Neat Glycerol to Lactic Acid Acs Catalysis. 6: 2014-2017. DOI: 10.1021/Acscatal.5B02732 |
0.621 |
|
2015 |
Zhang X, Lu Z, Foellmer LK, Williams TJ. Nitrogen-Based Ligands Accelerate Ammonia Borane Dehydrogenation with the Shvo Catalyst Organometallics. 34: 3732-3738. DOI: 10.1021/Acs.Organomet.5B00409 |
0.655 |
|
2014 |
Pennington-Boggio MK, Conley BL, Richmond MG, Williams TJ. Synthesis, Structure, and Conformational Dynamics of Rhodium and Iridium Complexes of Dimethylbis(2-pyridyl)borate. Polyhedron. 84: 24-31. PMID 25435645 DOI: 10.1016/J.Poly.2014.05.042 |
0.773 |
|
2014 |
Wu X, Dawsey AC, Siriwardena-Mahanama BN, Allen MJ, Williams TJ. A (Fluoroalkyl)Guanidine Modulates the Relaxivity of a Phosphonate-Containing T 1-Shortening Contrast Agent. Journal of Fluorine Chemistry. 168: 177-183. PMID 25431503 DOI: 10.1016/J.Jfluchem.2014.09.018 |
0.756 |
|
2014 |
Celaje JA, Pennington-Boggio MK, Flaig RW, Richmond MG, Williams TJ. Synthesis and Characterization of Dimethylbis(2-pyridyl)borate Nickel(II) Complexes: Unimolecular Square-Planar to Square-Planar Rotation around Nickel(II). Organometallics. 33: 2019-2026. PMID 24882919 DOI: 10.1021/Om500173J |
0.754 |
|
2014 |
Krylova VA, Djurovich PI, Conley BL, Haiges R, Whited MT, Williams TJ, Thompson ME. Control of emission colour with N-heterocyclic carbene (NHC) ligands in phosphorescent three-coordinate Cu(I) complexes. Chemical Communications (Cambridge, England). 50: 7176-9. PMID 24853355 DOI: 10.1039/C4Cc02037E |
0.742 |
|
2014 |
Lu Z, Williams TJ. A dual site catalyst for mild, selective nitrile reduction. Chemical Communications (Cambridge, England). 50: 5391-3. PMID 24409456 DOI: 10.1039/C3Cc47384H |
0.653 |
|
2014 |
Li V, Ghang YJ, Hooley RJ, Williams TJ. Non-covalent self assembly controls the relaxivity of magnetically active guests. Chemical Communications (Cambridge, England). 50: 1375-7. PMID 24346341 DOI: 10.1039/C3Cc48389D |
0.493 |
|
2013 |
Dawsey AC, Hathaway KL, Kim S, Williams TJ. Introductory Chemistry: A Molar Relaxivity Experiment in the High School Classroom. Journal of Chemical Education. 90: 922-925. PMID 23929983 DOI: 10.1021/Ed3006902 |
0.759 |
|
2013 |
Li V, Chang AY, Williams TJ. A noncovalent, fluoroalkyl coating monomer for phosphonate-covered nanoparticles. Tetrahedron. 69: 7741-7746. PMID 23913989 DOI: 10.1016/J.Tet.2013.05.092 |
0.482 |
|
2012 |
Lu Z, Conley BL, Williams TJ. A Three-Stage Mechanistic Model for Ammonia Borane Dehydrogenation by Shvo's Catalyst. Organometallics. 31: 6705-6714. PMID 23335832 DOI: 10.1021/Om300562D |
0.818 |
|
2012 |
Pennington-Boggio MK, Conley BL, Williams TJ. A Ruthenium-Catalyzed Coupling of Alkynes with 1,3-Diketones. Journal of Organometallic Chemistry. 716: 6-10. PMID 22923850 DOI: 10.1016/J.Jorganchem.2012.05.017 |
0.815 |
|
2012 |
Dawsey AC, Li V, Hamilton KC, Wang J, Williams TJ. Copper-catalyzed oxidation of azolines to azoles. Dalton Transactions (Cambridge, England : 2003). 41: 7994-8002. PMID 22460353 DOI: 10.1039/C2Dt00025C |
0.8 |
|
2012 |
Lu Z, Malinoski B, Flores AV, Conley BL, Guess D, Williams TJ. Alcohol dehydrogenation with a dual site ruthenium, Boron Catalyst occurs at ruthenium Catalysts. 2: 412-421. DOI: 10.3390/Catal2040412 |
0.786 |
|
2012 |
Wu X, Boz E, Sirkis AM, Chang AY, Williams TJ. Synthesis and phosphonate binding of guanidine-functionalized fluorinated amphiphiles Journal of Fluorine Chemistry. 135: 292-302. DOI: 10.1016/J.Jfluchem.2011.12.011 |
0.66 |
|
2011 |
Conley BL, Guess D, Williams TJ. A robust, air-stable, reusable ruthenium catalyst for dehydrogenation of ammonia borane. Journal of the American Chemical Society. 133: 14212-5. PMID 21827173 DOI: 10.1021/Ja2058154 |
0.758 |
|
2011 |
Williams TJ, Kershaw AD, Li V, Wu X. An Inversion Recovery NMR Kinetics Experiment. Journal of Chemical Education. 88: 665-669. PMID 21552343 DOI: 10.1021/Ed1006822 |
0.703 |
|
2011 |
Conley BL, Williams TJ. Dual site catalysts for hydride manipulation Comments On Inorganic Chemistry. 32: 195-218. DOI: 10.1080/02603594.2011.642087 |
0.776 |
|
2010 |
Conley BL, Williams TJ. Dehydrogenation of ammonia-borane by Shvo's catalyst. Chemical Communications (Cambridge, England). 46: 4815-7. PMID 20508879 DOI: 10.1039/C003157G |
0.76 |
|
2010 |
Wender PA, Sirois LE, Stemmler RT, Williams TJ. Highly efficient, facile, room temperature intermolecular [5 + 2] cycloadditions catalyzed by cationic rhodium(I): one step to cycloheptenes and their libraries. Organic Letters. 12: 1604-7. PMID 20196579 DOI: 10.1021/Ol100337M |
0.571 |
|
2010 |
Conley BL, Pennington-Boggio MK, Boz E, Williams TJ. Discovery, applications, and catalytic mechanisms of Shvo's catalyst. Chemical Reviews. 110: 2294-312. PMID 20095576 DOI: 10.1021/Cr9003133 |
0.784 |
|
2010 |
Conley BL, Williams TJ. Thermochemistry and molecular structure of a remarkable agostic interaction in a heterobifunctional ruthenium-boron complex. Journal of the American Chemical Society. 132: 1764-5. PMID 20088526 DOI: 10.1021/Ja909858A |
0.737 |
|
2010 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. ChemInform Abstract: Toward the Ideal Synthesis: New Transition Metal catalyzed Reactions Inspired by Novel Medicinal Leads Cheminform. 33: no-no. DOI: 10.1002/chin.200241295 |
0.835 |
|
2010 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. ChemInform Abstract: Toward the Ideal Synthesis: New Transition Metal catalyzed Reactions Inspired by Novel Medicinal Leads Cheminform. 33: no-no. DOI: 10.1002/chin.200241295 |
0.835 |
|
2010 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. ChemInform Abstract: Toward the Ideal Synthesis: New Transition Metal catalyzed Reactions Inspired by Novel Medicinal Leads Cheminform. 33: no-no. DOI: 10.1002/chin.200241295 |
0.835 |
|
2010 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. ChemInform Abstract: Toward the Ideal Synthesis: New Transition Metal catalyzed Reactions Inspired by Novel Medicinal Leads Cheminform. 33: no-no. DOI: 10.1002/chin.200241295 |
0.835 |
|
2009 |
Thorson MK, Klinkel KL, Wang J, Williams TJ. Mechanism of hydride abstraction by cyclopentadienone-ligated carbonylmetal complexes (M = Ru, Fe) European Journal of Inorganic Chemistry. 295-302. DOI: 10.1002/Ejic.200800975 |
0.433 |
|
2008 |
Williams TJ, Caffyn AJ, Hazari N, Oblad PF, Labinger JA, Bercaw JE. C-H bond activation by air-stable [(diimine)M(II)(mu2-OH)]2(2+) dimers (M = Pd, Pt). Journal of the American Chemical Society. 130: 2418-9. PMID 18237167 DOI: 10.1021/Ja076740Q |
0.79 |
|
2008 |
Bercaw JE, Hazari N, Williams TJ, Caffyn AJM, Oblad PF, Labinger JA. Carbon-hydrogen bond activation with platinum and palladium complexes Acs National Meeting Book of Abstracts. |
0.765 |
|
2007 |
Williams TJ, Labinger JA, Bercaw JE. Reactions of Indene and Indoles with Platinum Methyl Cations: Indene C-H Activation, Indole π vs. Nitrogen Lone-Pair Coordination. Organometallics. 26: 281-287. PMID 27087735 DOI: 10.1021/Om0606643 |
0.495 |
|
2007 |
Driver TG, Williams TJ, Labinger JA, Bercaw JE. C-H bond activation by dicationic platinum(II) complexes Organometallics. 26: 294-301. DOI: 10.1021/Om060792R |
0.697 |
|
2007 |
Williams TJ, Labinger JA, Bercaw JE. Reactions of indene and indoles with platinum methyl cations: Indene C-H activation, indole π versus nitrogen lone-pair coordination Organometallics. 26: 281-287. DOI: 10.1021/om0606643 |
0.495 |
|
2006 |
Wender PA, Paxton TJ, Williams TJ. Cyclopentadienone synthesis by rhodium(I)-catalyzed [3 + 2] cycloaddition reactions of cyclopropenones and alkynes. Journal of the American Chemical Society. 128: 14814-5. PMID 17105285 DOI: 10.1021/Ja065868P |
0.627 |
|
2006 |
Wender PA, Haustedt LO, Lim J, Love JA, Williams TJ, Yoon JY. Asymmetric catalysis of the [5 + 2] cycloaddition reaction of vinylcyclopropanes and pi-systems. Journal of the American Chemical Society. 128: 6302-3. PMID 16683779 DOI: 10.1021/Ja058590U |
0.741 |
|
2006 |
Wender P, Haustedt L, Lim J, Love J, Williams T, Yoon J. Asymmetric [5+2] Cycloaddition of Vinylcyclopropanes and π-Systems Synfacts. 2006: 0809-0809. DOI: 10.1055/S-2006-942016 |
0.605 |
|
2006 |
Wender P, Haustedt L, Lim J, Love J, Williams T, Yoon J. Asymmetric [5+2] Cycloaddition of Vinylcyclopropanes and π-Systems Synfacts. 2006: 0809-0809. DOI: 10.1055/S-2006-942016 |
0.605 |
|
2006 |
Wender P, Haustedt L, Lim J, Love J, Williams T, Yoon J. Asymmetric [5+2] Cycloaddition of Vinylcyclopropanes and π-Systems Synfacts. 2006: 0809-0809. DOI: 10.1055/S-2006-942016 |
0.605 |
|
2006 |
Wender P, Haustedt L, Lim J, Love J, Williams T, Yoon J. Asymmetric [5+2] Cycloaddition of Vinylcyclopropanes and π-Systems Synfacts. 2006: 0809-0809. DOI: 10.1055/S-2006-942016 |
0.605 |
|
2005 |
Wender PA, Gamber GG, Williams TJ. Rhodium(I)-Catalyzed [5+2], [6+2], and [5+2+1] Cycloadditions: New Reactions for Organic Synthesis Modern Rhodium-Catalyzed Organic Reactions. 263-299. DOI: 10.1002/3527604693.ch13 |
0.823 |
|
2004 |
Wender PA, Deschamps NM, Williams TJ. Intermolecular dienyl Pauson-Khand reaction. Angewandte Chemie (International Ed. in English). 43: 3076-9. PMID 15188486 DOI: 10.1002/Anie.200454117 |
0.809 |
|
2003 |
Wender PA, Baryza JL, Brenner SE, Clarke MO, Gamber GG, Horan JC, Jessop TC, Kan C, Pattabiraman K, Williams TJ. Inspirations from nature. New reactions, new therapeutic leads, and new drug delivery systems Pure and Applied Chemistry. 75: 143-155. DOI: 10.1351/Pac200375020143 |
0.772 |
|
2003 |
Wender PA, Love JA, Williams TJ. Rhodium-catalyzed [5+2] cycloaddition reactions in water Synlett. 1295-1298. DOI: 10.1055/S-2003-40357 |
0.716 |
|
2003 |
Wender PA, Baryza JL, Brenner SE, Clarke MO, Gamber GG, Horan JC, Jessop TC, Kan C, Pattabiraman K, Williams TJ. Inspirations from nature. New reactions, therapeutic leads, and drug delivery systems Pure and Applied Chemistry. 75: 143-155. |
0.755 |
|
2002 |
Wender PA, Williams TJ. [(arene)Rh(cod)]+ Complexes as catalysts for [5+2] cycloaddition reactions. Angewandte Chemie (International Ed. in English). 41: 4550-3. PMID 12458535 DOI: 10.1002/1521-3773(20021202)41:23<4550::Aid-Anie4550>3.0.Co;2-D |
0.634 |
|
2002 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025 |
0.857 |
|
2002 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025 |
0.857 |
|
2002 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025 |
0.857 |
|
2002 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025 |
0.857 |
|
2002 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025 |
0.857 |
|
2002 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025 |
0.857 |
|
2002 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025 |
0.857 |
|
2002 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025 |
0.857 |
|
2002 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025 |
0.857 |
|
2002 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025 |
0.857 |
|
2002 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025 |
0.857 |
|
2002 |
Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/Pac200274010025 |
0.851 |
|
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