Year |
Citation |
Score |
2024 |
Chen LM, Reisman SE. Enantioselective C(sp)-C(sp) Bond Construction by Ni Catalysis. Accounts of Chemical Research. 57: 751-762. PMID 38346006 DOI: 10.1021/acs.accounts.3c00775 |
0.351 |
|
2024 |
Gao Y, Jiang B, Friede NC, Hunter AC, Boucher DG, Minteer SD, Sigman MS, Reisman SE, Baran PS. Electrocatalytic Asymmetric Nozaki-Hiyama-Kishi Decarboxylative Coupling: Scope, Applications, and Mechanism. Journal of the American Chemical Society. PMID 38324710 DOI: 10.1021/jacs.3c13442 |
0.621 |
|
2023 |
Raghavan P, Haas BC, Ruos ME, Schleinitz J, Doyle AG, Reisman SE, Sigman MS, Coley CW. Dataset Design for Building Models of Chemical Reactivity. Acs Central Science. 9: 2196-2204. PMID 38161380 DOI: 10.1021/acscentsci.3c01163 |
0.611 |
|
2023 |
Barbor JP, Nair VN, Sharp KR, Lohrey TD, Dibrell SE, Shah TK, Walsh MJ, Reisman SE, Stoltz BM. Development of a Nickel-Catalyzed N-N Coupling for the Synthesis of Hydrazides. Journal of the American Chemical Society. 145: 15071-15077. PMID 37413695 DOI: 10.1021/jacs.3c04834 |
0.498 |
|
2023 |
Ware SD, Zhang W, Charboneau DJ, Klein CK, Reisman SE, See KA. Electrochemical Preparation of Sm(II) Reagent Facilitated by Weakly Coordinating Anions. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301045. PMID 37309269 DOI: 10.1002/chem.202301045 |
0.698 |
|
2023 |
Kerkovius JK, Wong AR, Mak VW, Reisman SE. A convergent fragment coupling strategy to access quaternary stereogenic centers. Chemical Science. 14: 4397-4400. PMID 37123185 DOI: 10.1039/d2sc07023e |
0.447 |
|
2022 |
Lacker CR, DeLano TJ, Chen EP, Kong J, Belyk KM, Piou T, Reisman SE. Enantioselective Synthesis of -Benzylic Heterocycles by Ni/Photoredox Dual Catalysis. Journal of the American Chemical Society. 144: 20190-20195. PMID 36288571 DOI: 10.1021/jacs.2c07917 |
0.351 |
|
2022 |
Turro RF, Brandstätter M, Reisman SE. Nickel-Catalyzed Reductive Alkylation of Heteroaryl Imines. Angewandte Chemie (International Ed. in English). PMID 35791274 DOI: 10.1002/anie.202207597 |
0.367 |
|
2022 |
Gnaim S, Bauer A, Zhang HJ, Chen L, Gannett C, Malapit CA, Hill DE, Vogt D, Tang T, Daley RA, Hao W, Zeng R, Quertenmont M, Beck WD, Kandahari E, ... ... Reisman SE, et al. Cobalt-electrocatalytic HAT for functionalization of unsaturated C-C bonds. Nature. 605: 687-695. PMID 35614246 DOI: 10.1038/s41586-022-04595-3 |
0.705 |
|
2022 |
Mendoza SD, Rombola M, Tao Y, Zuend SJ, Götz R, McLaughlin MJ, Reisman SE. Expanding the Chiral Monoterpene Pool: Enantioselective Diels-Alder Reactions of α-Acyloxy Enones. Organic Letters. 24: 3802-3806. PMID 35594569 DOI: 10.1021/acs.orglett.2c01343 |
0.784 |
|
2022 |
Holman KR, Stanko AM, Richter MJR, Feng SS, Gessesse MN, Reisman SE. Synthesis of Noraugustamine and Development of an Oxidative Heck/Aza-Wacker Cascade Cyclization. Organic Letters. 24: 3019-3023. PMID 35426682 DOI: 10.1021/acs.orglett.2c00948 |
0.381 |
|
2022 |
Grünenfelder DC, Navarro R, Wang H, Fastuca NJ, Butler JR, Reisman SE. Enantioselective Synthesis of (-)-C10-Hydroxyacutuminine. Angewandte Chemie (International Ed. in English). PMID 35112449 DOI: 10.1002/anie.202117480 |
0.391 |
|
2021 |
Wong AR, Fastuca NJ, Mak VW, Kerkovius JK, Stevenson SM, Reisman SE. Total Syntheses of the C Diterpenoid Alkaloids (-)-Talatisamine, (-)-Liljestrandisine, and (-)-Liljestrandinine by a Fragment Coupling Approach. Acs Central Science. 7: 1311-1316. PMID 34471676 DOI: 10.1021/acscentsci.1c00540 |
0.316 |
|
2021 |
DeLano TJ, Dibrell SE, Lacker CR, Pancoast AR, Poremba KE, Cleary L, Sigman MS, Reisman SE. Nickel-catalyzed asymmetric reductive cross-coupling of α-chloroesters with (hetero)aryl iodides. Chemical Science. 12: 7758-7762. PMID 34168828 DOI: 10.1039/d1sc00822f |
0.568 |
|
2021 |
Gao Y, Hill DE, Hao W, McNicholas BJ, Vantourout JC, Hadt RG, Reisman SE, Blackmond DG, Baran PS. Electrochemical Nozaki-Hiyama-Kishi Coupling: Scope, Applications, and Mechanism. Journal of the American Chemical Society. PMID 34128671 DOI: 10.1021/jacs.1c03007 |
0.612 |
|
2021 |
Nakayama Y, Maser MR, Okita T, Dubrovskiy AV, Campbell TL, Reisman SE. Total Synthesis of Ritterazine B. Journal of the American Chemical Society. PMID 33689345 DOI: 10.1021/jacs.1c01372 |
0.776 |
|
2021 |
Dibrell SE, Tao Y, Reisman SE. Synthesis of Complex Diterpenes: Strategies Guided by Oxidation Pattern Analysis. Accounts of Chemical Research. PMID 33621061 DOI: 10.1021/acs.accounts.0c00858 |
0.331 |
|
2020 |
Cowper NGW, Hesse MJ, Chan KM, Reisman SE. A copper-catalyzed asymmetric oxime propargylation enables the synthesis of the gliovirin tetrahydro-1,2-oxazine core. Chemical Science. 11: 11897-11901. PMID 34094417 DOI: 10.1039/d0sc04802j |
0.376 |
|
2020 |
Poremba KE, Dibrell SE, Reisman SE. Nickel-Catalyzed Enantioselective Reductive Cross-Coupling Reactions. Acs Catalysis. 10: 8237-8246. PMID 32905517 DOI: 10.1021/Acscatal.0C01842 |
0.415 |
|
2020 |
Reisman SE, Sarpong R, Sigman MS, Yoon TP. Organic Chemistry: A Call to Action for Diversity and Inclusion. Acs Central Science. 6: 1241-1247. PMID 32875064 DOI: 10.1021/Acs.Organomet.0C00519 |
0.653 |
|
2020 |
Reisman SE, Sarpong R, Sigman MS, Yoon TP. Organic Chemistry: A Call to Action for Diversity and Inclusion. Organic Letters. PMID 32806162 DOI: 10.1021/Acs.Orglett.0C02559 |
0.653 |
|
2020 |
Reisman SE, Sarpong R, Sigman MS, Yoon TP. Organic Chemistry: A Call to Action for Diversity and Inclusion. The Journal of Organic Chemistry. PMID 32806096 DOI: 10.1021/Acs.Joc.0C01607 |
0.662 |
|
2020 |
Dibrell SE, Maser MR, Reisman SE. SeO-Mediated Oxidative Transposition of Pauson-Khand Products. Journal of the American Chemical Society. 142: 6483-6487. PMID 32188246 DOI: 10.1021/Jacs.9B13818 |
0.333 |
|
2019 |
DeLano TJ, Reisman SE. Enantioselective Electroreductive Coupling of Alkenyl and Benzyl Halides via Nickel Catalysis. Acs Catalysis. 9: 6751-6754. PMID 32351776 DOI: 10.1021/Acscatal.9B01785 |
0.425 |
|
2019 |
Han A, Tao Y, Reisman SE. A 16-step synthesis of the isoryanodane diterpene (+)-perseanol. Nature. 573: 563-567. PMID 31554978 DOI: 10.1038/S41586-019-1580-X |
0.424 |
|
2019 |
Hofstra JL, Poremba KE, Shimozono A, Reisman SE. Ni-Catalyzed Conversion of Enol Triflates to Alkenyl Halides. Angewandte Chemie (International Ed. in English). PMID 31410936 DOI: 10.1002/Anie.201906815 |
0.419 |
|
2019 |
Beck JC, Lacker CR, Chapman LM, Reisman SE. A modular approach to prepare enantioenriched cyclobutanes: synthesis of (+)-rumphellaone A. Chemical Science. 10: 2315-2319. PMID 30881657 DOI: 10.1039/C8Sc05444D |
0.534 |
|
2019 |
Gabriel P, Xie L, Dixon DJ, Holman KR, Reisman SE. Iridium‐Catalyzed Reductive Coupling of Grignard Reagents and Tertiary Amides Organic Syntheses. 96: 511-527. DOI: 10.1002/0471264229.Os096.31 |
0.33 |
|
2018 |
Su JY, Grünenfelder DC, Takeuchi K, Reisman SE. Radical Deoxychlorination of Cesium Oxalates for the Synthesis of Alkyl Chlorides. Organic Letters. PMID 30062894 DOI: 10.1021/Acs.Orglett.8B02045 |
0.431 |
|
2018 |
Xu C, Han A, Reisman SE. An Oxidative Dearomatization Approach To Prepare the Pentacyclic Core of Ryanodol. Organic Letters. PMID 29897247 DOI: 10.1021/Acs.Orglett.8B01387 |
0.383 |
|
2018 |
Poremba KE, Kadunce NT, Suzuki N, Cherney AH, Reisman SE. Correction to "Nickel-Catalyzed Asymmetric Reductive Cross-Coupling To Access 1,1-Diarylalkanes". Journal of the American Chemical Society. PMID 29889504 DOI: 10.1021/Jacs.8B05247 |
0.339 |
|
2018 |
Chapman LM, Beck JC, Lacker CR, Wu L, Reisman SE. Evolution of a Strategy for the Enantioselective Total Synthesis of (+)-Psiguadial B. The Journal of Organic Chemistry. PMID 29728045 DOI: 10.1021/Acs.Joc.8B00728 |
0.501 |
|
2018 |
Farney EP, Feng SS, Schäfers F, Reisman SE. Total Synthesis of (+)-Pleuromutilin. Journal of the American Chemical Society. PMID 29323492 DOI: 10.1021/Jacs.7B13260 |
0.499 |
|
2018 |
Würfel H, Jakobi D, Lacker C, DeLano TJ, Reisman S. Syntheses of Substituted 2‐Cyano‐Benzothiazoles Organic Syntheses. 95: 177-191. DOI: 10.1002/0471264229.Os095.12 |
0.397 |
|
2017 |
Hofstra JL, Cherney AH, Ordner CM, Reisman SE. Synthesis of Enantioenriched Allylic Silanes via Nickel-Catalyzed Reductive Cross-Coupling. Journal of the American Chemical Society. PMID 29202243 DOI: 10.1021/Jacs.7B11707 |
0.473 |
|
2017 |
Xu C, Han A, Virgil SC, Reisman SE. Chemical Synthesis of (+)-Ryanodine and (+)-20-Deoxyspiganthine. Acs Central Science. 3: 278-282. PMID 28470044 DOI: 10.1021/Acscentsci.6B00361 |
0.426 |
|
2017 |
Poremba KE, Kadunce NT, Suzuki N, Cherney AH, Reisman SE. Nickel-Catalyzed Asymmetric Reductive Cross-Coupling To Access 1,1-Diarylalkanes. Journal of the American Chemical Society. PMID 28406620 DOI: 10.1021/Jacs.7B01705 |
0.446 |
|
2017 |
Suzuki N, Hofstra JL, Poremba KE, Reisman SE. Nickel-Catalyzed Enantioselective Cross-Coupling of N-Hydroxyphthalimide Esters with Vinyl Bromides. Organic Letters. PMID 28375631 DOI: 10.1021/Acs.Orglett.7B00793 |
0.404 |
|
2017 |
Wang H, Regan CJ, Codelli JA, Romanato P, Puchlopek-Dermenci AL, Reisman SE. Enantioselective Synthesis of (-)-Acetylapoaranotin. Organic Letters. PMID 28349698 DOI: 10.1021/Acs.Orglett.7B00418 |
0.544 |
|
2016 |
Chuang KV, Kieffer ME, Reisman SE. A Mild and General Larock Indolization Protocol for the Preparation of Unnatural Tryptophans. Organic Letters. PMID 27598827 DOI: 10.1021/Acs.Orglett.6B02477 |
0.417 |
|
2016 |
Chuang KV, Xu C, Reisman SE. A 15-step synthesis of (+)-ryanodol. Science (New York, N.Y.). 353: 912-5. PMID 27563092 DOI: 10.1126/Science.Aag1028 |
0.444 |
|
2016 |
Chapman LM, Beck JC, Wu L, Reisman SE. Enantioselective Total Synthesis of (+)-Psiguadial B. Journal of the American Chemical Society. PMID 27452034 DOI: 10.1021/Jacs.6B07229 |
0.533 |
|
2016 |
Daniels BE, Ni J, Reisman SE. Synthesis of Enantioenriched Indolines by a Conjugate Addition/Asymmetric Protonation/Aza-Prins Cascade Reaction. Angewandte Chemie (International Ed. in English). PMID 26844668 DOI: 10.1002/Anie.201510972 |
0.474 |
|
2015 |
Cherney AH, Kadunce NT, Reisman SE. Enantioselective and Enantiospecific Transition-Metal-Catalyzed Cross-Coupling Reactions of Organometallic Reagents To Construct C-C Bonds. Chemical Reviews. 115: 9587-652. PMID 26268813 DOI: 10.1021/Acs.Chemrev.5B00162 |
0.459 |
|
2015 |
Kadunce NT, Reisman SE. Nickel-Catalyzed Asymmetric Reductive Cross-Coupling between Heteroaryl Iodides and α-Chloronitriles. Journal of the American Chemical Society. PMID 26256474 DOI: 10.1021/Jacs.5B06466 |
0.399 |
|
2015 |
Jang KS, Nani RR, Kalli A, Levin S, Müller A, Hess S, Reisman SE, Clemons WM. A cationic cysteine-hydrazide as an enrichment tool for the mass spectrometric characterization of bacterial free oligosaccharides. Analytical and Bioanalytical Chemistry. PMID 26100547 DOI: 10.1007/S00216-015-8798-8 |
0.704 |
|
2014 |
Cherney AH, Reisman SE. Nickel-catalyzed asymmetric reductive cross-coupling between vinyl and benzyl electrophiles. Journal of the American Chemical Society. 136: 14365-8. PMID 25245492 DOI: 10.1021/Ja508067C |
0.4 |
|
2014 |
Wang H, Reisman SE. Enantioselective total synthesis of (-)-lansai B and (+)-nocardioazines A and B. Angewandte Chemie (International Ed. in English). 53: 6206-10. PMID 24777757 DOI: 10.1002/Anie.201402571 |
0.412 |
|
2014 |
Yeoman JTS, Cha JY, Mak VW, Reisman SE. A unified strategy for the synthesis of (-)-maoecrystal Z, (-)-trichorabdal A, and (-)-longikaurin E Tetrahedron. 70: 4070-4088. DOI: 10.1016/J.Tet.2014.03.071 |
0.405 |
|
2014 |
Cherney AH, Reisman SE. Pd-catalyzed Fukuyama cross-coupling of secondary organozinc reagents for the direct synthesis of unsymmetrical ketones Tetrahedron. 70: 3259-3265. DOI: 10.1016/J.Tet.2013.11.104 |
0.438 |
|
2014 |
Yeoman JT, Cha JY, Mak VW, Reisman SE. ChemInform Abstract: A Unified Strategy for the Synthesis of (-)-Maoecrystal Z, (-)-Trichorabdal A, and (-)-Longikaurin E. Cheminform. 45: no-no. DOI: 10.1002/chin.201445211 |
0.777 |
|
2013 |
Repka LM, Reisman SE. Recent developments in the catalytic, asymmetric construction of pyrroloindolines bearing all-carbon quaternary stereocenters. The Journal of Organic Chemistry. 78: 12314-20. PMID 24295135 DOI: 10.1021/Jo4017953 |
0.48 |
|
2013 |
Ni J, Wang H, Reisman SE. Direct, Enantioselective Synthesis of Pyrroloindolines and Indolines From Simple Indole Derivatives. Tetrahedron. 69: 5622-5633. PMID 24039305 DOI: 10.1016/J.Tet.2013.04.003 |
0.495 |
|
2013 |
Yeoman JT, Mak VW, Reisman SE. A unified strategy to ent-kauranoid natural products: total syntheses of (-)-trichorabdal A and (-)-longikaurin E. Journal of the American Chemical Society. 135: 11764-7. PMID 23886049 DOI: 10.1021/Ja406599A |
0.794 |
|
2013 |
Nani RR, Reisman SE. α-Diazo-β-ketonitriles: uniquely reactive substrates for arene and alkene cyclopropanation. Journal of the American Chemical Society. 135: 7304-11. PMID 23642221 DOI: 10.1021/Ja401610P |
0.731 |
|
2013 |
Cherney AH, Kadunce NT, Reisman SE. Catalytic asymmetric reductive acyl cross-coupling: synthesis of enantioenriched acyclic α,α-disubstituted ketones. Journal of the American Chemical Society. 135: 7442-5. PMID 23634932 DOI: 10.1021/Ja402922W |
0.44 |
|
2013 |
Codelli JA, Reisman SE. Chemistry. Pactamycin made easy. Science (New York, N.Y.). 340: 152-3. PMID 23580517 DOI: 10.1126/Science.1236882 |
0.331 |
|
2013 |
Kieffer ME, Chuang KV, Reisman SE. Copper-catalyzed diastereoselective arylation of tryptophan derivatives: total synthesis of (+)-naseseazines A and B. Journal of the American Chemical Society. 135: 5557-60. PMID 23540731 DOI: 10.1021/Ja4023557 |
0.501 |
|
2013 |
Cherney AH, Kadunce NT, Reisman SE. Nickel-Catalyzed Asymmetric Direct Reductive Acyl Cross-Coupling Reaction Synfacts. 9: 855-855. DOI: 10.1055/S-0033-1339353 |
0.407 |
|
2012 |
Lim AD, Codelli JA, Reisman SE. Catalytic Asymmetric Synthesis of Highly Substituted Pyrrolizidines. Chemical Science (Royal Society of Chemistry : 2010). 4: 650-654. PMID 23565328 DOI: 10.1039/C2Sc21617E |
0.473 |
|
2012 |
Kieffer ME, Chuang KV, Reisman SE. A Copper-Catalyzed Arylation of Tryptamines for the Direct Synthesis of Aryl Pyrroloindolines. Chemical Science (Royal Society of Chemistry : 2010). 3: 3170-3174. PMID 23105962 DOI: 10.1039/C2Sc20914D |
0.443 |
|
2012 |
Yeoman JT, Reisman SE. Organic chemistry: Single molecules put a ring on it. Nature. 490: 179-80. PMID 23060182 DOI: 10.1038/490179A |
0.794 |
|
2012 |
Navarro R, Reisman SE. Rapid construction of the aza-propellane core of acutumine via a photochemical [2 + 2] cycloaddition reaction. Organic Letters. 14: 4354-7. PMID 22891873 DOI: 10.1021/Ol3017963 |
0.481 |
|
2012 |
Kieffer ME, Repka LM, Reisman SE. Enantioselective synthesis of tryptophan derivatives by a tandem Friedel-Crafts conjugate addition/asymmetric protonation reaction. Journal of the American Chemical Society. 134: 5131-7. PMID 22390403 DOI: 10.1021/Ja209390D |
0.483 |
|
2012 |
Codelli JA, Puchlopek AL, Reisman SE. Enantioselective total synthesis of (-)-acetylaranotin, a dihydrooxepine epidithiodiketopiperazine. Journal of the American Chemical Society. 134: 1930-3. PMID 22023250 DOI: 10.1021/Ja209354E |
0.532 |
|
2011 |
Chuang KV, Navarro R, Reisman SE. Short, enantioselective total syntheses of (-)-8-demethoxyrunanine and (-)-cepharatines A, C, and D. Angewandte Chemie (International Ed. in English). 50: 9447-51. PMID 21948444 DOI: 10.1002/Anie.201104487 |
0.372 |
|
2011 |
Cha JY, Yeoman JT, Reisman SE. A concise total synthesis of (-)-maoecrystal Z. Journal of the American Chemical Society. 133: 14964-7. PMID 21877709 DOI: 10.1021/Ja2073356 |
0.812 |
|
2011 |
Reisman SE. Medicinal chemistry: New lead for pain treatment. Nature. 473: 458-9. PMID 21614069 DOI: 10.1038/473458A |
0.305 |
|
2011 |
Levin S, Nani RR, Reisman SE. Enantioselective total synthesis of (+)-salvileucalin B. Journal of the American Chemical Society. 133: 774-6. PMID 21174417 DOI: 10.1021/Ja110192B |
0.798 |
|
2011 |
Reisman SE, Nani RR, Levin S. Buchner and beyond: Arene cyclopropanation as applied to natural product total synthesis Synlett. 2437-2442. DOI: 10.1055/S-0031-1289520 |
0.793 |
|
2011 |
Cha JY, Yeoman JTS, Reisman SE. Synthesis of (-)-Maoecrystal Z Synfacts. 2011: 1271-1271. DOI: 10.1055/S-0031-1289337 |
0.447 |
|
2011 |
Levin S, Nani RR, Reisman SE. Enantioselective Synthesis of (+)-SalvileucalinB Synfacts. 2011: 590-590. DOI: 10.1055/S-0030-1260369 |
0.502 |
|
2011 |
Chuang KV, Navarro R, Reisman SE. Benzoquinone-derived sulfinyl imines as versatile intermediates for alkaloid synthesis: Total synthesis of (-)-3-demethoxyerythratidinone Chemical Science. 2: 1086-1089. DOI: 10.1039/C1Sc00095K |
0.553 |
|
2011 |
Reisman SE, Nani RR, Levin S. ChemInform Abstract: Buchner and Beyond: Arene Cyclopropanation as Applied to Natural Product Total Synthesis Cheminform. 43: no-no. DOI: 10.1002/chin.201204240 |
0.768 |
|
2010 |
Repka LM, Ni J, Reisman SE. Enantioselective synthesis of pyrroloindolines by a formal [3 + 2] cycloaddition reaction. Journal of the American Chemical Society. 132: 14418-20. PMID 20873714 DOI: 10.1021/Ja107328G |
0.544 |
|
2010 |
Freeman DB, Holubec AA, Weiss MW, Dixon JA, Kakefuda A, Ohtsuka M, Inoue M, Vaswani RG, Ohki H, Doan BD, Reisman SE, Stoltz BM, Day JJ, Tao RN, Dieterich NA, et al. Welwitindolinone C synthetic studies. Construction of the welwitindolinone carbon skeleton via a transannular nitrone cycloaddition. Tetrahedron. 66: 6647-6655. PMID 20733933 DOI: 10.1016/J.Tet.2010.04.131 |
0.723 |
|
2010 |
Levin S, Nani RR, Reisman SE. Rapid assembly of the salvileucalin B norcaradiene core. Organic Letters. 12: 780-3. PMID 20088588 DOI: 10.1021/Ol902848K |
0.782 |
|
2008 |
Reisman SE, Doyle AG, Jacobsen EN. Enantioselective thiourea-catalyzed additions to oxocarbenium ions. Journal of the American Chemical Society. 130: 7198-9. PMID 18479086 DOI: 10.1021/Ja801514M |
0.681 |
|
2008 |
Reisman SE, Ready JM, Weiss MM, Hasuoka A, Hirata M, Tamaki K, Ovaska TV, Smith CJ, Wood JL. Evolution of a synthetic strategy: total synthesis of (+/-)-welwitindolinone A isonitrile. Journal of the American Chemical Society. 130: 2087-100. PMID 18198870 DOI: 10.1021/Ja076663Z |
0.809 |
|
2008 |
Reisman SE, Doyle AG, Jacobsen EN. Enantioselective Additions to Oxocarbenium Ions via AnionBinding Synfacts. 2008: 1106-1106. DOI: 10.1055/S-2008-1078145 |
0.472 |
|
2006 |
Reisman SE, Ready JM, Hasuoka A, Smith CJ, Wood JL. Total synthesis of (+/-)-welwitindolinone a isonitrile. Journal of the American Chemical Society. 128: 1448-9. PMID 16448105 DOI: 10.1002/CHIN.200626167 |
0.748 |
|
2006 |
Wood J, Reisman S, Ready J, Hasuoka A, Smith C. Synthesis of (±)-Welwitindolinone A Isonitrile Synfacts. 2006: 0642-0642. DOI: 10.1055/S-2006-941823 |
0.631 |
|
2004 |
Ready JM, Reisman SE, Hirata M, Weiss MM, Tamaki K, Ovaska TV, Wood JL. A mild and efficient synthesis of oxindoles: progress towards the synthesis of welwitindolinone A isonitrile. Angewandte Chemie (International Ed. in English). 43: 1270-2. PMID 14991796 DOI: 10.1002/Anie.200353282 |
0.8 |
|
2002 |
Ravi Kumar JS, O'Sullivan MF, Reisman SE, Hulford CA, Ovaska TV. Facile approach to the bicyclo[5.3.0]decane ring system; efficient synthesis of (±)-7-epi-β-bulnesene Tetrahedron Letters. 43: 1939-1941. DOI: 10.1016/S0040-4039(02)00171-5 |
0.44 |
|
2001 |
Ovaska TV, Reisman SE, Flynn MA. Facile entry to the tetracyclic 5-7-6-3 tigliane ring system. Organic Letters. 3: 115-7. PMID 11429851 DOI: 10.1021/Ol006823A |
0.464 |
|
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