Year |
Citation |
Score |
2017 |
Lopchuk JM, Fjelbye K, Kawamata Y, Malins LR, Pan CM, Gianatassio R, Wang J, Prieto L, Bradow J, Brandt TA, Collins MR, Elleraas J, Ewanicki J, Farrell W, Fadeyi OO, et al. Strain-Release Heteroatom Functionalization: Development, Scope, and Stereospecificity. Journal of the American Chemical Society. PMID 28140573 DOI: 10.1021/Jacs.6B13229 |
0.678 |
|
2016 |
Gianatassio R, Lopchuk JM, Wang J, Pan CM, Malins LR, Prieto L, Brandt TA, Collins MR, Gallego GM, Sach NW, Spangler JE, Zhu H, Zhu J, Baran PS. Strain-release amination. Science (New York, N.Y.). 351: 241-246. PMID 26816372 DOI: 10.1126/Science.Aad6252 |
0.674 |
|
2015 |
Montgomery WL, Lopchuk JM, Gribble GW, Jasinski JP. Synthesis, crystal structures, and dft calculations of three new cyano(Phenylsulfonyl)indoles and a key synthetic precursor compound Crystals. 5: 376-393. DOI: 10.3390/cryst5030376 |
0.446 |
|
2015 |
Lopchuk JM, Song M, Butler B, Gribble GW. Synthesis of Heteroaryl-Substituted Pyrroles via the 1,3-Dipolar Cycloaddition of Unsymmetrical Münchnones and Nitrovinylheterocycles Synthesis (Germany). DOI: 10.1055/S-0034-1380720 |
0.531 |
|
2014 |
Cherney EC, Lopchuk JM, Green JC, Baran PS. A unified approach to ent-atisane diterpenes and related alkaloids: synthesis of (-)-methyl atisenoate, (-)-isoatisine, and the hetidine skeleton. Journal of the American Chemical Society. 136: 12592-5. PMID 25159015 DOI: 10.1021/Ja507321J |
0.55 |
|
2014 |
Lopchuk JM, Gribble GW, Jasinski JP. Methyl 1-benzyl-5-methyl-2,4-diphenyl-1H-pyrrole-3-carboxyl-ate. Acta Crystallographica. Section E, Structure Reports Online. 70: o338-9. PMID 24765032 DOI: 10.1107/S1600536814003316 |
0.522 |
|
2014 |
Lopchuk JM, Gribble GW, Jasinski JP. Methyl 1-benzyl-5-methyl-2,4-diphenyl-1H-pyrrole-3-carboxylate Acta Crystallographica Section E: Structure Reports Online. 70: o338-o339. DOI: 10.1107/S1600536814003316 |
0.403 |
|
2014 |
Lopchuk JM, Gribble GW. Total synthesis of atorvastatin via a late-stage, regioselective 1,3-dipolar münchnone cycloaddition Tetrahedron Letters. DOI: 10.1016/J.Tetlet.2014.12.104 |
0.527 |
|
2014 |
Lopchuk JM, Gribble GW. The reaction of arynes with münchnones: Synthesis of isoindoles and azaisoindoles Tetrahedron Letters. 55: 2809-2812. DOI: 10.1016/J.Tetlet.2014.03.055 |
0.538 |
|
2014 |
Lopchuk JM. Five-membered ring systems: Pyrroles and benzo analogs Progress in Heterocyclic Chemistry. 26: 151-192. DOI: 10.1016/B978-0-08-096807-0.00006-3 |
0.391 |
|
2013 |
Lopchuk JM, Gribble GW, Millikan SP, Jasinski JP. Bruceolline J: 2-hy-droxy-3,3-dimethyl-2,3-di-hydro-cyclo-penta-[b]indol-1(4H)-one. Acta Crystallographica. Section E, Structure Reports Online. 69: o1351-2. PMID 24109417 DOI: 10.1107/S1600536813020527 |
0.503 |
|
2013 |
Lopchuk JM, Hughes RP, Gribble GW. What controls regiochemistry in 1,3-dipolar cycloadditions of münchnones with nitrostyrenes? Organic Letters. 15: 5218-21. PMID 24073889 DOI: 10.1021/Ol402385V |
0.434 |
|
2013 |
Lopchuk JM, Gribble GW, Jasinski JP. Bruceolline D: 3,3-dimethyl-1H,4H-cyclo-penta-[b]indol-2(3H)-one. Acta Crystallographica. Section E, Structure Reports Online. 69: o1043. PMID 24046619 DOI: 10.1107/S1600536813014955 |
0.501 |
|
2013 |
Lopchuk JM, Green IL, Badenock JC, Gribble GW. A short, protecting group-free total synthesis of bruceollines D, E, and J Organic Letters. 15: 4485-4487. PMID 23937106 DOI: 10.1021/Ol402042F |
0.657 |
|
2013 |
Lopchuk JM, Gribble GW, Millikan SP, Jasinski JP. Bruceolline J: 2-hydroxy-3,3-dimethyl-2,3-dihydrocyclopenta[b]indol-1(4H)- one Acta Crystallographica Section E: Structure Reports Online. 69: o1351-o1352. DOI: 10.1107/S1600536813020527 |
0.408 |
|
2013 |
Lopchuk JM, Gribble GW, Jasinski JP. Bruceolline D: 3,3-dimethyl-1H,4H-cyclopenta[b]indol-2(3H)-one Acta Crystallographica Section E: Structure Reports Online. 69: o1043. DOI: 10.1107/S1600536813014955 |
0.394 |
|
2013 |
Lopchuk JM, Montgomery WL, Jasinski JP, Gorjifard S, Gribble GW. Manganese(III)-mediated oxidative radical addition of malonates to 2-cyanoindoles Tetrahedron Letters. 54: 6142-6145. DOI: 10.1016/J.Tetlet.2013.09.012 |
0.483 |
|
2013 |
Lopchuk JM. Five-membered ring systems. Pyrroles and benzo analogs. Progress in Heterocyclic Chemistry. 25: 137-182. DOI: 10.1016/B978-0-08-099406-2.00007-8 |
0.394 |
|
2011 |
Sporn MB, Liby KT, Yore MM, Fu L, Lopchuk JM, Gribble GW. New synthetic triterpenoids: Potent agents for prevention and treatment of tissue injury caused by inflammatory and oxidative stress Journal of Natural Products. 74: 537-545. PMID 21309592 DOI: 10.1021/Np100826Q |
0.477 |
|
2011 |
Lopchuk JM, Gribble GW. A convenient 1,3-dipolar cycloaddition approach to pyridylpyrroles Tetrahedron Letters. 52: 4106-4108. DOI: 10.1016/J.Tetlet.2011.05.111 |
0.528 |
|
2010 |
Lopchuk JM, Gribble GW. Synthesis of 2-and 3-indolylpyrroles via 1,3-dipolar cycloadditions of münchnones and nitroalkenes Heterocycles. 82: 1617-1631. DOI: 10.3987/Com-10-S(E)125 |
0.55 |
|
Low-probability matches (unlikely to be authored by this person) |
2020 |
Chandrachud PP, Wojtas L, Lopchuk JM. Decarboxylative Amination: Diazirines as Single and Double Electrophilic Nitrogen Transfer Reagents. Journal of the American Chemical Society. PMID 33332115 DOI: 10.1021/jacs.0c09403 |
0.297 |
|
2022 |
Shultz ZP, Scattolin T, Wojtas L, Lopchuk JM. Stereospecific α-(hetero)arylation of sulfoximines and sulfonimidamides. Nature Synthesis. 1: 170-179. PMID 35415722 DOI: 10.1038/s44160-021-00011-2 |
0.296 |
|
2024 |
Teng S, Shultz ZP, Shan C, Wojtas L, Lopchuk JM. Asymmetric synthesis of sulfoximines, sulfonimidoyl fluorides and sulfonimidamides enabled by an enantiopure bifunctional S(VI) reagent. Nature Chemistry. PMID 38238465 DOI: 10.1038/s41557-023-01419-3 |
0.253 |
|
2018 |
Ji Y, Wojtas L, Lopchuk JM. An improved, gram-scale synthesis of protected 3-haloazetidines: rapid diversified synthesis of azetidine-3-carboxylic acids Arkivoc. 2018: 195-214. DOI: 10.24820/ark.5550190.p010.549 |
0.248 |
|
2021 |
Maharaj V, Chandrachud PP, Che W, Wojtas L, Lopchuk JM. Photodecarboxylative Amination of Redox-Active Esters with Diazirines. Organic Letters. 23: 8838-8842. PMID 34747619 DOI: 10.1021/acs.orglett.1c03344 |
0.223 |
|
2011 |
Lopchuk JM. Recent advances in the synthesis of aspidosperma-type alkaloids Progress in Heterocyclic Chemistry. 23: 1-25. DOI: 10.1016/B978-0-08-096805-6.00001-2 |
0.202 |
|
2022 |
Karim RM, Yang L, Chen L, Bikowitz MJ, Lu J, Grassie D, Shultz ZP, Lopchuk JM, Chen J, Schönbrunn E. Discovery of Dual TAF1-ATR Inhibitors and Ligand-Induced Structural Changes of the TAF1 Tandem Bromodomain. Journal of Medicinal Chemistry. PMID 35191694 DOI: 10.1021/acs.jmedchem.1c01999 |
0.076 |
|
Hide low-probability matches. |