Year |
Citation |
Score |
2023 |
Chen M, Ventura AM, Das S, Ibrahim AF, Zimmerman PM, Montgomery J. Oxidative Cross Dehydrogenative Coupling of -Heterocycles with Aldehydes through C()-H Functionalization. Journal of the American Chemical Society. 145: 20176-20181. PMID 37672664 DOI: 10.1021/jacs.3c06532 |
0.325 |
|
2022 |
Rand AW, Chen M, Montgomery J. Investigations into mechanism and origin of regioselectivity in the metallaphotoredox-catalyzed α-arylation of -alkylbenzamides. Chemical Science. 13: 10566-10573. PMID 36277638 DOI: 10.1039/d2sc01962k |
0.363 |
|
2022 |
Xiao J, Montgomery J. Nickel-Catalyzed Defluorinative Coupling of Aliphatic Aldehydes with Trifluoromethyl Alkenes. Acs Catalysis. 12: 2463-2471. PMID 35992737 DOI: 10.1021/acscatal.1c05801 |
0.452 |
|
2021 |
Xiao J, Li Z, Montgomery J. Nickel-Catalyzed Decarboxylative Coupling of Redox-Active Esters with Aliphatic Aldehydes. Journal of the American Chemical Society. 143: 21234-21240. PMID 34894690 DOI: 10.1021/jacs.1c11170 |
0.442 |
|
2021 |
Cruz CL, Montgomery J. Nickel-catalyzed reductive coupling of unactivated alkyl bromides and aliphatic aldehydes. Chemical Science. 12: 11995-12000. PMID 34667565 DOI: 10.1039/d1sc03712a |
0.437 |
|
2020 |
Sati G, Martin J, Xu Y, Malakar T, Zimmerman PM, Montgomery J. Fluoride Migration Catalysis Enables Simple, Stereoselective, and Iterative Glycosylation. Journal of the American Chemical Society. PMID 32207615 DOI: 10.1021/Jacs.0C03165 |
0.408 |
|
2020 |
Jenkins AD, Robo MT, Zimmerman PM, Montgomery J. Nickel-Catalyzed Three-Component Cycloadditions of Enoates, Alkynes, and Aldehydes. The Journal of Organic Chemistry. PMID 32004432 DOI: 10.1021/Acs.Joc.9B02446 |
0.651 |
|
2020 |
Rand AW, Yin H, Xu L, Giacoboni J, Martin-Montero R, Romano C, Montgomery J, Martin R. Dual Catalytic Platform for Enabling sp3 α C–H Arylation and Alkylation of Benzamides Acs Catalysis. 10: 4671-4676. DOI: 10.1021/Acscatal.0C01318 |
0.414 |
|
2019 |
Rand AW, Montgomery J. Catalytic reduction of aryl trialkylammonium salts to aryl silanes and arenes. Chemical Science. 10: 5338-5344. PMID 31191891 DOI: 10.1039/C9Sc01083A |
0.519 |
|
2019 |
Kim HK, Mane MV, Montgomery J, Baik MH. The Mechanism of Copper-Catalyzed Trifunctionalization of Terminal Allenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31038842 DOI: 10.1002/Chem.201900673 |
0.472 |
|
2018 |
Cañellas S, Montgomery J, Pericàs MA. Nickel-Catalyzed Reductive [2+2] Cycloaddition of Alkynes. Journal of the American Chemical Society. PMID 30517785 DOI: 10.1021/Jacs.8B09677 |
0.499 |
|
2018 |
Nett AJ, Cañellas S, Higuchi Y, Robo MT, Kochkodan JM, Haynes MT, Kampf JW, Montgomery J. Stable, Well-Defined Nickel(0) Catalysts for Catalytic C-C and C-N Bond Formation. Acs Catalysis. 8: 6606-6611. PMID 30079273 DOI: 10.1021/Acscatal.8B02187 |
0.411 |
|
2018 |
Wiensch EM, Montgomery J. Nickel-Catalyzed Amination of Silyloxyarenes via C-O Bond Activation. Angewandte Chemie (International Ed. in English). PMID 29949675 DOI: 10.1002/Anie.201806790 |
0.496 |
|
2018 |
Shimkin KW, Montgomery J. Synthesis of Tetrasubstituted Alkenes by Tandem Metallacycle Formation/Cross-Electrophile Coupling. Journal of the American Chemical Society. PMID 29800523 DOI: 10.1021/Jacs.8B04637 |
0.496 |
|
2017 |
Gilbert MM, DeMars MD, Yang S, Grandner JM, Wang S, Wang H, Narayan ARH, Sherman DH, Houk KN, Montgomery J. Synthesis of Diverse 11- and 12-Membered Macrolactones from a Common Linear Substrate Using a Single Biocatalyst. Acs Central Science. 3: 1304-1310. PMID 29296671 DOI: 10.1021/Acscentsci.7B00450 |
0.371 |
|
2017 |
Wang H, Lu G, Sormunen GJ, Malik HA, Liu P, Montgomery J. NHC Ligands Tailored for Simultaneous Regio- and Enantiocontrol in Nickel-Catalyzed Reductive Couplings. Journal of the American Chemical Society. PMID 28621131 DOI: 10.1021/Jacs.7B04583 |
0.838 |
|
2017 |
Nett AJ, Montgomery J, Zimmerman PM. Entrances, Traps, and Rate-Controlling Factors for Nickel-Catalyzed C–H Functionalization Acs Catalysis. 7: 7352-7362. DOI: 10.1021/Acscatal.7B02919 |
0.461 |
|
2017 |
Wiensch EM, Todd DP, Montgomery J. Silyloxyarenes as Versatile Coupling Substrates Enabled by Nickel-Catalyzed C–O Bond Cleavage Acs Catalysis. 7: 5568-5571. DOI: 10.1021/Acscatal.7B02025 |
0.465 |
|
2016 |
Kerchner HA, Montgomery J. Synthesis of Secondary and Tertiary Alkylboranes via Formal Hydroboration of Terminal and 1,1-Disubstituted Alkenes. Organic Letters. PMID 27786484 DOI: 10.1021/Acs.Orglett.6B03090 |
0.474 |
|
2016 |
Zhao W, Montgomery J. Cascade Copper-Catalyzed 1,2,3-Trifunctionalization of Terminal Allenes. Journal of the American Chemical Society. PMID 27438071 DOI: 10.1021/Jacs.6B05216 |
0.438 |
|
2016 |
Huard K, Gosset JR, Montgomery JI, Gilbert AM, Hayward MM, Magee TV, Cabral S, Uccello DP, Bahnck KB, Brown JA, Purkal J, Gorgoglione MF, Lanba A, Futatsugi K, Herr M, et al. Optimization of a dicarboxylic series for in vivo inhibition of citrate transport by the solute carrier 13 (SLC13) family. Journal of Medicinal Chemistry. PMID 26734723 DOI: 10.1021/Acs.Jmedchem.5B01752 |
0.696 |
|
2015 |
Todd DP, Thompson BB, Nett AJ, Montgomery J. Deoxygenative C-C Bond-Forming Processes via a Net Four-Electron Reductive Coupling. Journal of the American Chemical Society. 137: 12788-91. PMID 26436636 DOI: 10.1021/Jacs.5B08448 |
0.625 |
|
2015 |
Zhao W, Montgomery J. Functionalization of Styrenes by Copper-Catalyzed Borylation/ ortho-Cyanation and Silver-Catalyzed Annulation Processes. Angewandte Chemie (International Ed. in English). PMID 26332432 DOI: 10.1002/Anie.201507303 |
0.495 |
|
2015 |
Narayan AR, Jiménez-Osés G, Liu P, Negretti S, Zhao W, Gilbert MM, Ramabhadran RO, Yang YF, Furan LR, Li Z, Podust LM, Montgomery J, Houk KN, Sherman DH. Enzymatic hydroxylation of an unactivated methylene C-H bond guided by molecular dynamics simulations. Nature Chemistry. 7: 653-60. PMID 26201742 DOI: 10.1038/Nchem.2285 |
0.795 |
|
2015 |
Miller ZD, Dorel R, Montgomery J. Regiodivergent and Stereoselective Hydrosilylation of 1,3-Disubstituted Allenes. Angewandte Chemie (International Ed. in English). PMID 26079290 DOI: 10.1002/Anie.201503521 |
0.617 |
|
2015 |
Nett AJ, Zhao W, Zimmerman PM, Montgomery J. Highly Active Nickel Catalysts for C-H Functionalization Identified through Analysis of Off-Cycle Intermediates. Journal of the American Chemical Society. 137: 7636-9. PMID 26057139 DOI: 10.1021/Jacs.5B04548 |
0.391 |
|
2015 |
Walk JT, Buchan ZA, Montgomery J. Sugar Silanes: Versatile Reagents for Stereocontrolled Glycosylation via Intramolecular Aglycone Delivery. Chemical Science (Royal Society of Chemistry : 2010). 6: 3448-3453. PMID 26000163 DOI: 10.1039/C5Sc00810G |
0.793 |
|
2015 |
Jackson EP, Malik HA, Sormunen GJ, Baxter RD, Liu P, Wang H, Shareef AR, Montgomery J. Mechanistic Basis for Regioselection and Regiodivergence in Nickel-Catalyzed Reductive Couplings. Accounts of Chemical Research. 48: 1736-45. PMID 25965694 DOI: 10.1021/Acs.Accounts.5B00096 |
0.827 |
|
2015 |
Wang H, Negretti S, Knauff AR, Montgomery J. Exo-selective reductive macrocyclization of ynals. Organic Letters. 17: 1493-6. PMID 25746060 DOI: 10.1021/Acs.Orglett.5B00381 |
0.804 |
|
2015 |
Jackson EP, Montgomery J. Regiocontrol in catalytic reductive couplings through alterations of silane rate dependence. Journal of the American Chemical Society. 137: 958-63. PMID 25531576 DOI: 10.1021/Ja511778A |
0.584 |
|
2014 |
Haynes MT, Liu P, Baxter RD, Nett AJ, Houk KN, Montgomery J. Dimer involvement and origin of crossover in nickel-catalyzed aldehyde-alkyne reductive couplings. Journal of the American Chemical Society. 136: 17495-504. PMID 25401337 DOI: 10.1021/Ja508909U |
0.693 |
|
2014 |
Miller ZD, Montgomery J. Regioselective allene hydroarylation via one-pot allene hydrosilylation/Pd-catalyzed cross-coupling. Organic Letters. 16: 5486-9. PMID 25275880 DOI: 10.1021/Ol502766Q |
0.613 |
|
2014 |
Negretti S, Narayan AR, Chiou KC, Kells PM, Stachowski JL, Hansen DA, Podust LM, Montgomery J, Sherman DH. Directing group-controlled regioselectivity in an enzymatic C-H bond oxygenation. Journal of the American Chemical Society. 136: 4901-4. PMID 24627965 DOI: 10.1021/Ja5016052 |
0.796 |
|
2013 |
Partridge KM, Bader SJ, Buchan ZA, Taylor CE, Montgomery J. A streamlined strategy for aglycone assembly and glycosylation. Angewandte Chemie (International Ed. in English). 52: 13647-50. PMID 24151089 DOI: 10.1002/Anie.201307680 |
0.805 |
|
2013 |
Miller ZD, Li W, Belderrain TR, Montgomery J. Regioselective allene hydrosilylation catalyzed by N-heterocyclic carbene complexes of nickel and palladium. Journal of the American Chemical Society. 135: 15282-5. PMID 24079389 DOI: 10.1021/Ja407749W |
0.613 |
|
2013 |
Lage ML, Bader SJ, Sa-Ei K, Montgomery J. Chemoselective hydrosilylation of hydroxyketones. Tetrahedron. 69: 5609-5613. PMID 23997314 DOI: 10.1016/J.Tet.2013.04.055 |
0.826 |
|
2012 |
Shareef AR, Sherman DH, Montgomery J. Nickel-Catalyzed Regiodivergent Approach to Macrolide Motifs. Chemical Science (Royal Society of Chemistry : 2010). 3: 892-895. PMID 22737401 DOI: 10.1039/C2Sc00866A |
0.759 |
|
2012 |
Li W, Montgomery J. Ligand-guided pathway selection in nickel-catalyzed couplings of enals and alkynes. Chemical Communications (Cambridge, England). 48: 1114-6. PMID 22159624 DOI: 10.1039/C2Cc17073F |
0.489 |
|
2011 |
Montgomery J. Chemistry. High-throughput discovery of new chemical reactions. Science (New York, N.Y.). 333: 1387-8. PMID 21903798 DOI: 10.1126/Science.1210735 |
0.347 |
|
2011 |
Jenkins AD, Herath A, Song M, Montgomery J. Synthesis of cyclopentenols and cyclopentenones via nickel-catalyzed reductive cycloaddition. Journal of the American Chemical Society. 133: 14460-6. PMID 21819132 DOI: 10.1021/Ja206722T |
0.764 |
|
2011 |
Thompson BB, Montgomery J. Enone-alkyne reductive coupling: a versatile entry to substituted pyrroles. Organic Letters. 13: 3289-91. PMID 21657241 DOI: 10.1021/Ol201133N |
0.637 |
|
2011 |
ElDouhaibi AS, Kassab RM, Song M, Montgomery J. Nickel-catalyzed cyclizations of enoates and chiral allenes: an approach to domoic acid. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 6326-9. PMID 21538617 DOI: 10.1002/Chem.201100444 |
0.81 |
|
2011 |
Liu P, Montgomery J, Houk KN. Ligand steric contours to understand the effects of N-heterocyclic carbene ligands on the reversal of regioselectivity in Ni-catalyzed reductive couplings of alkynes and aldehydes. Journal of the American Chemical Society. 133: 6956-9. PMID 21506540 DOI: 10.1021/Ja202007S |
0.446 |
|
2011 |
Baxter RD, Montgomery J. Mechanistic study of nickel-catalyzed ynal reductive cyclizations through kinetic analysis. Journal of the American Chemical Society. 133: 5728-31. PMID 21438642 DOI: 10.1021/Ja200867D |
0.682 |
|
2011 |
Jenkins AD, Herath A, Song M, Montgomery J. Ni-Catalyzed Reductive Cycloaddition Synfacts. 2011: 1194-1194. DOI: 10.1055/S-0031-1289222 |
0.415 |
|
2010 |
Li W, Chen N, Montgomery J. Regioselective nickel-catalyzed reductive couplings of enones and allenes. Angewandte Chemie (International Ed. in English). 49: 8712-6. PMID 20931589 DOI: 10.1002/Anie.201004740 |
0.486 |
|
2010 |
Phillips JH, Montgomery J. Mechanistic insights into nickel-catalyzed cycloisomerizations. Organic Letters. 12: 4556-9. PMID 20843015 DOI: 10.1021/Ol101852W |
0.426 |
|
2010 |
Malik HA, Sormunen GJ, Montgomery J. A general strategy for regiocontrol in nickel-catalyzed reductive couplings of aldehydes and alkynes. Journal of the American Chemical Society. 132: 6304-5. PMID 20394367 DOI: 10.1021/Ja102262V |
0.834 |
|
2010 |
Malik HA, Sormunen GJ, Montgomery J. Regiocontrol in the Nickel-Catalyzed Aldehyde-AlkyneReductive Coupling Synfacts. 2010: 899-899. DOI: 10.1055/S-0030-1257777 |
0.717 |
|
2010 |
Ni Y, Kassab RM, Chevliakov MV, Montgomery J. Syntheses of Isodomoic Acids G and H Synfacts. 2010: 382-382. DOI: 10.1055/S-0029-1219454 |
0.759 |
|
2010 |
Malik HA, Baxter RD, Montgomery J. Nickel-Catalyzed Reductive Couplings and Cyclizations Catalysis Without Precious Metals. 181-212. DOI: 10.1002/9783527631582.ch8 |
0.786 |
|
2009 |
Sa-Ei K, Montgomery J. Diastereoselective Nickel-Catalyzed Reductive Couplings of Aminoaldehydes and Alkynylsilanes: Application to the Synthesis of D-erythro-Sphingosine. Tetrahedron. 65: 6707-6711. PMID 20640041 DOI: 10.1016/J.Tet.2009.05.029 |
0.839 |
|
2009 |
Malik HA, Chaulagain MR, Montgomery J. Cooperativity of regiochemistry control strategies in reductive couplings of propargyl alcohols and aldehydes. Organic Letters. 11: 5734-7. PMID 19919081 DOI: 10.1021/Ol902561R |
0.818 |
|
2009 |
Ni Y, Kassab RM, Chevliakov MV, Montgomery J. Total syntheses of isodomoic acids G and H: an exercise in tetrasubstituted alkene synthesis. Journal of the American Chemical Society. 131: 17714-8. PMID 19899794 DOI: 10.1021/Ja907931U |
0.798 |
|
2009 |
Li W, Herath A, Montgomery J. Evolution of efficient strategies for enone-alkyne and enal-alkyne reductive couplings. Journal of the American Chemical Society. 131: 17024-9. PMID 19883082 DOI: 10.1021/Ja9083607 |
0.398 |
|
2009 |
Li S, Chaulagain MR, Knauff AR, Podust LM, Montgomery J, Sherman DH. Selective oxidation of carbolide C-H bonds by an engineered macrolide P450 mono-oxygenase. Proceedings of the National Academy of Sciences of the United States of America. 106: 18463-8. PMID 19833867 DOI: 10.1073/Pnas.0907203106 |
0.796 |
|
2009 |
Buchan ZA, Bader SJ, Montgomery J. Ketone hydrosilylation with sugar silanes followed by intramolecular aglycone delivery: an orthogonal glycosylation strategy. Angewandte Chemie (International Ed. in English). 48: 4840-4. PMID 19492383 DOI: 10.1002/Anie.200901666 |
0.806 |
|
2008 |
Anzai Y, Li S, Chaulagain MR, Kinoshita K, Kato F, Montgomery J, Sherman DH. Functional analysis of MycCI and MycG, cytochrome P450 enzymes involved in biosynthesis of mycinamicin macrolide antibiotics. Chemistry & Biology. 15: 950-9. PMID 18804032 DOI: 10.1016/J.Chembiol.2008.07.014 |
0.795 |
|
2008 |
Baxter RD, Montgomery J. Dehydrogenative cyclocondensation of aldehydes, alkynes, and dialkylsilanes. Journal of the American Chemical Society. 130: 9662-3. PMID 18598032 DOI: 10.1021/Ja803774S |
0.663 |
|
2008 |
Herath A, Montgomery J. Highly chemoselective and stereoselective synthesis of z-enol silanes. Journal of the American Chemical Society. 130: 8132-3. PMID 18540581 DOI: 10.1021/Ja802844V |
0.538 |
|
2008 |
Chrovian CC, Knapp-Reed B, Montgomery J. Total synthesis of aigialomycin D: surprising chemoselectivity dependence on alkyne structure in nickel-catalyzed cyclizations. Organic Letters. 10: 811-4. PMID 18254635 DOI: 10.1021/Ol702961V |
0.819 |
|
2008 |
Herath A, Li W, Montgomery J. Fully intermolecular nickel-catalyzed three-component couplings via internal redox. Journal of the American Chemical Society. 130: 469-71. PMID 18081296 DOI: 10.1021/Ja0781846 |
0.534 |
|
2008 |
Chrovian CC, Knapp-Reed B, Montgomery J. Synthesis of Aigialomycin D Synfacts. 2008: 788-788. DOI: 10.1055/S-2008-1077895 |
0.777 |
|
2008 |
Herath A, Li W, Montgomery J. Three-Component Couplings via Internal Redox Synfacts. 2008: 414-414. DOI: 10.1055/S-2008-1042814 |
0.311 |
|
2007 |
Liu L, Montgomery J. [3+2] cycloaddition reactions of cyclopropyl imines with enones. Organic Letters. 9: 3885-7. PMID 17760449 DOI: 10.1021/Ol071376L |
0.541 |
|
2007 |
Chaulagain MR, Sormunen GJ, Montgomery J. New N-heterocyclic carbene ligand and its application in asymmetric nickel-catalyzed aldehyde/alkyne reductive couplings. Journal of the American Chemical Society. 129: 9568-9. PMID 17628066 DOI: 10.1021/Ja072992F |
0.836 |
|
2007 |
Herath A, Thompson BB, Montgomery J. Catalytic intermolecular reductive coupling of enones and alkynes. Journal of the American Chemical Society. 129: 8712-3. PMID 17590001 DOI: 10.1021/Ja073300Q |
0.648 |
|
2007 |
Chrovian CC, Montgomery J. Surprising role of aryl halides in nickel-catalyzed reductive aldol reactions. Organic Letters. 9: 537-40. PMID 17249806 DOI: 10.1021/Ol063028+ |
0.842 |
|
2007 |
Herath A, Thompson BB, Montgomery J. Nickel-Catalyzed Intermolecular Reductive Coupling of Enones and Alkynes Synfacts. 2007: 1092-1092. DOI: 10.1055/S-2007-968937 |
0.632 |
|
2007 |
Montgomery J, Sormunen GJ. Nickel-catalyzed reductive couplings of aldehydes and alkynes Topics in Current Chemistry. 279: 1-23. DOI: 10.1007/128_2007_139 |
0.835 |
|
2006 |
Herath A, Montgomery J. Catalytic intermolecular enal-alkyne [3 + 2] reductive cycloadditions. Journal of the American Chemical Society. 128: 14030-1. PMID 17061877 DOI: 10.1021/Ja0660249 |
0.451 |
|
2006 |
Sa-ei K, Montgomery J. Highly diastereoselective preparation of anti-1,2-diols by catalytic addition of alkynylsilanes to alpha-silyloxyaldehydes. Organic Letters. 8: 4441-3. PMID 16986920 DOI: 10.1021/Ol061579U |
0.819 |
|
2006 |
Liu L, Montgomery J. Dimerization of cyclopropyl ketones and crossed reactions of cyclopropyl ketones with enones as an entry to five-membered rings. Journal of the American Chemical Society. 128: 5348-9. PMID 16620099 DOI: 10.1021/Ja0602187 |
0.504 |
|
2006 |
Ni Y, Montgomery J. Synthetic studies and mechanistic insight in nickel-catalyzed [4+2+1] cycloadditions. Journal of the American Chemical Society. 128: 2609-14. PMID 16492045 DOI: 10.1021/Ja057741Q |
0.485 |
|
2006 |
Montgomery J, Chaulagain M, Mahandru G. Ni-Catalyzed Hydrosilylation of Alkynes Synfacts. 2006: 1050-1050. DOI: 10.1055/S-2006-949304 |
0.795 |
|
2006 |
ElDouhaibi AS, Lozanov M, Montgomery J. A multicomponent approach to substituted benzenes involving sequential nickel-catalyzed reactions Tetrahedron. 62: 11460-11469. DOI: 10.1016/J.Tet.2006.06.068 |
0.827 |
|
2006 |
Chaulagain MR, Mahandru GM, Montgomery J. Alkyne hydrosilylation catalyzed by nickel complexes of N-heterocyclic carbenes Tetrahedron. 62: 7560-7566. DOI: 10.1016/J.Tet.2006.03.120 |
0.824 |
|
2005 |
Knapp-Reed B, Mahandru GM, Montgomery J. Access to macrocyclic endocyclic and exocyclic allylic alcohols by nickel-catalyzed reductive cyclization of ynals. Journal of the American Chemical Society. 127: 13156-7. PMID 16173738 DOI: 10.1021/Ja054590I |
0.798 |
|
2005 |
Song M, Montgomery J. Nickel-catalyzed couplings and cyclizations involving allenes, aldehydes, and organozincs Tetrahedron. 61: 11440-11448. DOI: 10.1016/J.Tet.2005.08.066 |
0.684 |
|
2004 |
Ni Y, Montgomery J. An efficient [4 + 2 + 1] entry to seven-membered rings. Journal of the American Chemical Society. 126: 11162-3. PMID 15355092 DOI: 10.1021/Ja046147Y |
0.439 |
|
2004 |
Montgomery J. Nickel-catalyzed reductive cyclizations and couplings. Angewandte Chemie (International Ed. in English). 43: 3890-908. PMID 15274210 DOI: 10.1002/Anie.200300634 |
0.498 |
|
2004 |
Mahandru GM, Liu G, Montgomery J. Ligand-dependent scope and divergent mechanistic behavior in nickel-catalyzed reductive couplings of aldehydes and alkynes. Journal of the American Chemical Society. 126: 3698-9. PMID 15038707 DOI: 10.1021/Ja049644N |
0.824 |
|
2004 |
Hratchian HP, Chowdhury SK, Gutiérrez-García VM, Amarasinghe KKD, Heeg MJ, Schlegel HB, Montgomery J. Combined experimental and computational investigation of the mechanism of nickel-catalyzed three-component addition processes Organometallics. 23: 4636-4646. DOI: 10.1021/Om049471A |
0.606 |
|
2004 |
Mahandru GM, Liu G, Montgomery J. Ligand-Dependent Scope and Divergent Mechanistic Behavior in Nickel-Catalyzed Reductive Couplings of Aldehydes and Alkynes [J. Am. Chem. Soc.2004,126, 3698−3699]. Journal of the American Chemical Society. 126: 15316-15316. DOI: 10.1021/Ja044394W |
0.815 |
|
2003 |
Subburaj K, Montgomery J. A new catalytic conjugate addition/aldol strategy that avoids preformed metalated nucleophiles. Journal of the American Chemical Society. 125: 11210-1. PMID 16220938 DOI: 10.1021/Ja0362048 |
0.729 |
|
2003 |
Mahandru GM, Skauge AR, Chowdhury SK, Amarasinghe KK, Heeg MJ, Montgomery J. Cascade cyclizations and couplings involving nickel enolates. Journal of the American Chemical Society. 125: 13481-5. PMID 14583044 DOI: 10.1021/Ja037423W |
0.825 |
|
2003 |
Ni Y, Amarasinghe KK, Ksebati B, Montgomery J. First total synthesis and stereochemical definition of isodomoic acid G. Organic Letters. 5: 3771-3. PMID 14507227 DOI: 10.1021/Ol0355783 |
0.837 |
|
2002 |
Montgomery J, Song M. Preparation of homoallylic alcohols by nickel-catalyzed cyclizations of allenyl aldehydes. Organic Letters. 4: 4009-11. PMID 12423073 DOI: 10.1021/Ol026670M |
0.652 |
|
2002 |
Amarasinghe KK, Montgomery J. Enantioselective total synthesis of (+)-testudinariol a using a new nickel-catalyzed allenyl aldehyde cyclization. Journal of the American Chemical Society. 124: 9366-7. PMID 12167019 DOI: 10.1021/Ja027148Y |
0.84 |
|
2002 |
Ni Y, Amarasinghe KK, Montgomery J. Nickel-catalyzed cyclizations and couplings with vinylzirconium reagents. Organic Letters. 4: 1743-5. PMID 12000288 DOI: 10.1021/Ol025812+ |
0.841 |
|
2002 |
Lozanov M, Montgomery J. A new two-step four-component synthesis of highly functionalized cyclohexenols by sequential nickel-catalyzed couplings. Journal of the American Chemical Society. 124: 2106-7. PMID 11878951 DOI: 10.1021/Ja0175845 |
0.84 |
|
2002 |
Fornicola RS, Subburaj K, Montgomery J. A new entry to the isogeissoschizoid skeleton. Organic Letters. 4: 615-7. PMID 11843605 DOI: 10.1021/Ol017213T |
0.832 |
|
2002 |
Montgomery J, Amarasinghe KKD, Chowdhury SK, Oblinger E, Seo J, Savchenko AV. Nickel-catalyzed cyclizations of alkynyl enones and alkynyl enals Pure and Applied Chemistry. 74: 129-133. DOI: 10.1351/Pac200274010129 |
0.831 |
|
2001 |
Amarasinghe KKD, Chowdhury SK, Heeg MJ, Montgomery J. Structure of an η1 nickel O-enolate: Mechanistic implications in catalytic enyne cyclizations Organometallics. 20: 370-372. DOI: 10.1021/Om0010013 |
0.542 |
|
2001 |
Lozanov M, Montgomery J. Nickel-catalyzed preparation of stereodefined allylic alcohols using silicon-tethered ynals Tetrahedron Letters. 42: 3259-3261. DOI: 10.1016/S0040-4039(01)00461-0 |
0.799 |
|
2000 |
Montgomery J. Nickel-catalyzed cyclizations, couplings, and cycloadditions involving three reactive components Accounts of Chemical Research. 33: 467-473. PMID 10913235 DOI: 10.1021/Ar990095D |
0.484 |
|
2000 |
Tang XQ, Montgomery J. Nickel-catalyzed preparation of bicyclic heterocycles: Total synthesis of (+)-allopumiliotoxin 267A, (+)-allopumiliotoxin 339A, and (+)-allopumiliotoxin 339B Journal of the American Chemical Society. 122: 6950-6954. DOI: 10.1021/Ja001440T |
0.413 |
|
2000 |
Chowdhury SK, Amarasinghe KKD, Heeg MJ, Montgomery J. Diverse reactivity manifolds of alkynyl enone- and alkynyl enal-derived nickelacycles discovery of nickel-promoted [3+2] and [2+1] cycloadditions [6] Journal of the American Chemical Society. 122: 6775-6776. DOI: 10.1021/Ja0012624 |
0.586 |
|
1999 |
Qi X, Montgomery J. New three-component synthesis of 1,3-dienes employing nickel catalysis Journal of Organic Chemistry. 64: 9310-9313. DOI: 10.1021/Jo9912810 |
0.421 |
|
1999 |
Seo J, Fain H, Blanc JB, Montgomery J. Nickel-catalyzed cyclizations of enoate equivalents: Application to the synthesis of angular triquinanes Journal of Organic Chemistry. 64: 6060-6065. DOI: 10.1021/Jo9908389 |
0.512 |
|
1999 |
Chevliakov MV, Montgomery J. A stereodivergent approach to (-)-α-kainic acid and (+)-α-allokainic acid utilizing the complementarity of alkyne and allene cyclizations Journal of the American Chemical Society. 121: 11139-11143. DOI: 10.1021/Ja993069J |
0.818 |
|
1999 |
Tang XQ, Montgomery J. Nickel catalysis in the stereoselective preparation of quinolizidine, pyrrolizidine, and indolizidine alkaloids: Total synthesis of (+)- allopumiliotoxin 267A Journal of the American Chemical Society. 121: 6098-6099. DOI: 10.1021/Ja990997+ |
0.356 |
|
1999 |
Seo J, Chui HMP, Heeg MJ, Montgomery J. Novel chemoselectivity and stereochemical aspects of nickel-catalyzed [2 + 2 + 2] cycloadditions Journal of the American Chemical Society. 121: 476-477. DOI: 10.1021/Ja983081W |
0.508 |
|
1999 |
Fornicola RS, Montgomery J. Convenient preparation of amino acid derivatives with two 13C labels Tetrahedron Letters. 40: 8337-8341. DOI: 10.1016/S0040-4039(99)01783-9 |
0.779 |
|
1998 |
Chevliakov MV, Montgomery J. Nickel and Palladium Catalysis in the Stereoselective Synthesis of Functionalized Pyrrolidines: Enantioselective Formal Synthesis of (+)-α-Allokainic Acid. Angewandte Chemie (International Ed. in English). 37: 3144-3146. PMID 29711307 DOI: 10.1002/(Sici)1521-3773(19981204)37:22<3144::Aid-Anie3144>3.0.Co;2-Y |
0.837 |
|
1998 |
Fornicola RS, Oblinger E, Montgomery J. A New Synthesis of α-Amino Acid Derivatives Employing Methyl Nitroacetate as a Versatile Glycine Template The Journal of Organic Chemistry. 63: 3528-3529. DOI: 10.1021/Jo980477H |
0.786 |
|
1998 |
Montgomery J, Seo J. Synthetic studies and mechanistic observations in nickel-catalyzed polycyclizations Tetrahedron. 54: 1131-1144. DOI: 10.1016/S0040-4020(97)10213-7 |
0.473 |
|
1998 |
Chevliakov MV, Montgomery J. Nickel and palladium catalysis in the stereoselective synthesis of functionalized pyrrolidines: Enantioselective formal synthesis of (+)-α- allokainic acid Angewandte Chemie - International Edition. 37: 3144-3146. DOI: 10.1002/(SICI)1521-3773(19981204)37:22<3144::AID-ANIE3144>3.0.CO;2-Y |
0.825 |
|
1998 |
Chevliakov M, Montgomery J. Nickel- und Palladiumkatalyse bei der stereoselektiven Synthese funktionalisierter Pyrrolidine: enantioselektive formale Synthese von (+)-α-Allokainsäure Angewandte Chemie. 110: 3346-3348. DOI: 10.1002/(Sici)1521-3757(19981116)110:22<3346::Aid-Ange3346>3.0.Co;2-Z |
0.778 |
|
1997 |
Oblinger E, Montgomery J. A new stereoselective method for the preparation of allylic alcohols Journal of the American Chemical Society. 119: 9065-9066. DOI: 10.1021/Ja9719182 |
0.791 |
|
1997 |
Montgomery J, Oblinger E, Savchenko AV. Nickel-catalyzed organozinc-promoted carbocyclizations of electron-deficient alkenes with tethered unsaturation Journal of the American Chemical Society. 119: 4911-4920. DOI: 10.1021/Ja9702125 |
0.81 |
|
1997 |
Montgomery J, Chevliakov MV, Brielmann HL. Nickel-catalyzed heterocycle construction with stereoselective exocyclic alkene introduction Tetrahedron. 53: 16449-16462. DOI: 10.1016/S0040-4020(97)01027-2 |
0.845 |
|
1996 |
Savchenko AV, Montgomery J. Organozinc/Nickel(0)-Promoted Cyclizations of Bis-Enones. The Journal of Organic Chemistry. 61: 1562-1563. PMID 11667020 DOI: 10.1021/Jo960166B |
0.416 |
|
1996 |
Montgomery J, Savchenko AV. Nickel-catalyzed cyclizations of alkynyl enones with concomitant stereoselective tri- or tetrasubstituted alkene introduction Journal of the American Chemical Society. 118: 2099-2100. DOI: 10.1021/Ja952026+ |
0.577 |
|
1996 |
Montgomery J, Seo J, Chui HMP. Competition between insertion and conjugate addition in nickel-catalyzed couplings of enones with unsaturated functional groups Tetrahedron Letters. 37: 6839-6842. DOI: 10.1016/0040-4039(96)01528-6 |
0.526 |
|
1995 |
Montgomery J, Savchenko AV, Zhao Y. Convenient preparation of bis-enones and bis-enoates from cycloalkenes The Journal of Organic Chemistry. 60: 5699-5701. DOI: 10.1021/Jo00122A066 |
0.399 |
|
1995 |
Barr DA, Dorrity MJ, Grigg R, Hargreaves S, Malone JF, Montgomery J, Redpath J, Stevenson P, Thornton-Pett M. X=Y-ZH compounds as potential 1,3-dipoles. Part 43. Metal ion catalysed asymmetric 1,3-dipolar cycloaddition reactions of imines and menthyl acrylate Tetrahedron. 51: 273-294. DOI: 10.1016/0040-4020(94)00940-V |
0.335 |
|
1993 |
Montgomery J, Overman LE. Introduction of the 2-(phenylthio)ethyl, 2-(phenylsulfinyl)ethyl, and 2,2-bis(phenylthio)ethyl substituents into cyclic ketones The Journal of Organic Chemistry. 58: 6476-6479. DOI: 10.1021/Jo00075A054 |
0.599 |
|
1993 |
Montgomery J, Overman LE. Introduction of the 2-(phenylthio)ethyl, 2-(phenylsulfinyl)ethyl, and 2,2-bis(phenylthio)ethyl substituents into cyclic ketones Journal of Organic Chemistry. 58: 6476-6479. |
0.362 |
|
1991 |
Hegedus LS, Montgomery J, Narukawa Y, Snustad DC. A contribution to the confusion surrounding the reaction of ketenes with imines to produce β-lactams. A comparison of stereoselectivity dependence on the method of ketene generation: Acid chloride/triethylamine vs photolysis of chromium-carbene complexes Journal of the American Chemical Society. 113: 5784-5791. DOI: 10.1021/Ja00015A036 |
0.622 |
|
1990 |
Hegedus LS, Schultze LM, Montgomery J. Synthesis and properties of (O-acyl imidato)carbene complexes of chromium, molybdenum, and tungsten [Erratum to document cited in CA111(13):115461d] Organometallics. 9: 542-542. DOI: 10.1021/Om00116A041 |
0.521 |
|
1990 |
Montgomery J, Wieber GM, Hegedus LS. Synthesis of optically active ene carbamates from chromium carbene complexes: Use in paladium(II)-assisted synthesis of relays to (+)-thienamycin Journal of the American Chemical Society. 112: 6255-6263. DOI: 10.1021/Ja00173A012 |
0.562 |
|
1989 |
Hegedus LS, Schultze LM, Montgomery J. Synthesis and properties of (O-acyl imidato)carbene complexes of chromium, molybdenum, and tungsten Organometallics. 8: 2189-2195. DOI: 10.1021/Om00111A015 |
0.512 |
|
1961 |
Montgomery J, Thomas H, Schaeffer H. Correction- Synthesis of Potential Anticancer Agents. XXVIII. Simple Esters of 6-Mercaptopurine Ribonucleotide. Journal of Organic Chemistry. 26: 5260-5260. DOI: 10.1021/Jo01070A628 |
0.355 |
|
1961 |
Montgomery J, Thomas H. Correction- Synthesis of Potential Anticancer Agents. XXVII. The Ribonucleotides of 6-Mercaptopurine and 8-Azaguanine Journal of Organic Chemistry. 26: 5260-5260. DOI: 10.1021/Jo01070A627 |
0.307 |
|
1959 |
Balsiger R, Jones D, Montgomery J. Notes- Synthesis of Potential Anticancer Agents. XVIII. Analogs of Carbamoyl Phosphate The Journal of Organic Chemistry. 24: 434-436. DOI: 10.1021/Jo01085A616 |
0.313 |
|
1959 |
Montgomery J, Hewson K, Struck R, Shealy Y. A Convenient Synthesis of 4(5)-Amino-5(4)-imidazolecarboxamide Hydrochloride The Journal of Organic Chemistry. 24: 256-257. DOI: 10.1021/Jo01084A630 |
0.405 |
|
Show low-probability matches. |