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Wei, Lin-Li, Hsung, Richard P., Sklenicka, Heather M., Gerasyuto, Aleksey I. (2001) A Novel and Highly Stereoselective Intramolecular Formal [3+3] Cycloaddition Reaction of Vinylogous Amides Tethered withα,β-Unsaturated Aldehydes: A Formal Total Synthesis of (+)-Gephyrotoxin. Angewandte Chemie, 113 (8). 1564-1566 doi:10.1002/1521-3757(20010417)113:8<1564::aid-ange1564>3.0.co;2-j

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Reference TypeJournal (article/letter/editorial)
TitleA Novel and Highly Stereoselective Intramolecular Formal [3+3] Cycloaddition Reaction of Vinylogous Amides Tethered withα,β-Unsaturated Aldehydes: A Formal Total Synthesis of (+)-Gephyrotoxin
JournalAngewandte Chemie
AuthorsWei, Lin-LiAuthor
Hsung, Richard P.Author
Sklenicka, Heather M.Author
Gerasyuto, Aleksey I.Author
Year2001 (April 17)Volume113
Issue8
PublisherWiley
DOIdoi:10.1002/1521-3757(20010417)113:8<1564::aid-ange1564>3.0.co;2-jSearch in ResearchGate
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Mindat Ref. ID7298076Long-form Identifiermindat:1:5:7298076:1
GUID0
Full ReferenceWei, Lin-Li, Hsung, Richard P., Sklenicka, Heather M., Gerasyuto, Aleksey I. (2001) A Novel and Highly Stereoselective Intramolecular Formal [3+3] Cycloaddition Reaction of Vinylogous Amides Tethered withα,β-Unsaturated Aldehydes: A Formal Total Synthesis of (+)-Gephyrotoxin. Angewandte Chemie, 113 (8). 1564-1566 doi:10.1002/1521-3757(20010417)113:8<1564::aid-ange1564>3.0.co;2-j
Plain TextWei, Lin-Li, Hsung, Richard P., Sklenicka, Heather M., Gerasyuto, Aleksey I. (2001) A Novel and Highly Stereoselective Intramolecular Formal [3+3] Cycloaddition Reaction of Vinylogous Amides Tethered withα,β-Unsaturated Aldehydes: A Formal Total Synthesis of (+)-Gephyrotoxin. Angewandte Chemie, 113 (8). 1564-1566 doi:10.1002/1521-3757(20010417)113:83.0.co;2-j
In(2001, April) Angewandte Chemie Vol. 113 (8) Wiley

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Wei, Lin-Li, Hsung, Richard P., Sklenicka, Heather M., Gerasyuto, Aleksey I. (2001) A Novel and Highly Stereoselective Intramolecular Formal [3+3] Cycloaddition Reaction of Vinylogous Amides Tethered withα,β-Unsaturated Aldehydes: A Formal Total Synthesis of (+)-Gephyrotoxin. Angewandte Chemie International Edition, 40 (8). 1516-1518 doi:10.1002/1521-3773(20010417)40:8<1516::aid-anie1516>3.0.co;2-v
Sklenicka, Heather M., Hsung, Richard P., Wei, Lin-Li, McLaughlin, Michael J., Gerasyuto, Aleksey I., Degen, Shane J. (2000) Highly Stereoselective Formal [3 + 3] Cycloaddition Reactions of Chiral Vinylogous Amides with α,β-Unsaturated Iminiums. Organic Letters, 2. 1161-1164 doi:10.1021/ol000049+
Sklenicka, Heather M., Hsung, Richard P., McLaughlin, Michael J., Wei, Lin-li, Gerasyuto, Aleksey I., Brennessel, William B. (2002) Stereoselective Formal [3 + 3] Cycloaddition Approach tocis-1-Azadecalins and Synthesis of (−)-4a,8a-diepi-Pumiliotoxin C. Evidence for the First Highly Stereoselective 6π-Electron Electrocyclic Ring Closures of 1-Azatrienes. Journal Of The American Chemical Society, 124 (35) 10435-10442 doi:10.1021/ja020698b
Hsung, Richard P., Wei, Lin-Li, Sklenicka, Heather M., Douglas, Christopher J., McLaughlin, Michael J., Mulder, Jason A., Yao, Letitia J. (1999) Formal Cycloaddition Reactions of Vinylogous Amides with α,β-Unsaturated Iminiums. A Strategy for Constructing Piperidinyl Heterocycles. Organic Letters, 1. 509-512 doi:10.1021/ol990107v
Scott, Jack D., Williams, Robert M. (2001) Total Synthesis of (−)-Tetrazomine and Determination of Its Stereochemistry. Angewandte Chemie, 113 (8). 1511-1513 doi:10.1002/1521-3757(20010417)113:8<1511::aid-ange1511>3.0.co;2-a
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