Synthesis of Chiral Sulfinyl-Substituted 1-Indolyl Enones and Asymmetric Conjugate Addition by an Arylcopper Reagent
Author:
Affiliation:
1. Gifu Pharmaceutical University
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb/52/6/52_6_733/_pdf
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1. 1,6-Asymmetric Induction during the Conjugate Addition of Arylcopper Reagents to a Chiral Sulfinyl-Substituted Pyrrolyl .ALPHA., .BETA.-Unsaturated Amide.
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4. New synthesis of the antitumor 6H-pyrido[4,3-b]carbazole alkaloid ellipticine
5. Generation and reactions of 3-lithio-1-(phenylsulfonyl)indole
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2. Diastereoselective hydrogenation of α,β-unsaturated but-2-enamides to access the chiral 3-(p-tolyl) butanoic acids;Tetrahedron Letters;2017-01
3. The Sulfinyl Group as a Remote Chiral Auxiliary in Stereoselective Conjugate Additions of Alkyl Groups to α-Methylidene Carbonyl Compounds Initiated by Et3B/O2;European Journal of Organic Chemistry;2013-02-07
4. Metalation of Indole;Topics in Heterocyclic Chemistry;2010
5. Asymmetric Diels-Alder Reaction of 2-(p-Tolylsulfinyl)-1-indolyl a,b-Unsaturated Enones;HETEROCYCLES;2006
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