Novel Enantioselective Approach to γ-Lactams from Chiral Enol Ethers: Synthesis of (−)-Statine
Author:
Affiliation:
1. Université Joseph Fourier de Grenoble, Chimie Recherche (LEDSS), Domaine Universitaire, BP 53X, 38041 Grenoble Cedex, France
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo961035d
Reference15 articles.
1. Asymmetric induction in the cycloaddition reaction of dichloroketene with chiral enol ethers. A versatile approach to optically active cyclopentenone derivatives.
2. Enantioselective ring construction through asymmetric olefin-ketene cycloaddition. A highly enantiocontrolled approach to (-)-.alpha.-cuparenone and (+)-.beta.-cuparenone
3. Novel, enantioselective lactone construction. First synthesis of methylenolactocin, antitumor antibiotic from Penicillium sp
4. Synthesis and absolute stereochemistry of (-)-protolichesterinic acid, antitumor antibiotic lactone from Cetraria islandica
5. Chiral Enol Ethers in Asymmetric Synthesis: Preparation of the .beta.-Oxygenated Lactones (-)-Blastmycinolactol, (+)-Blastmycinone, (-)-NFX-2, and (+)-Antimycinone
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