Development of efficient Lewis acid catalysts for intramolecular cycloaddition reactions of ester-tethered substrates-Reference-Cited by-同舟云学术

Development of efficient Lewis acid catalysts for intramolecular cycloaddition reactions of ester-tethered substrates

Published:2007 Issue:3 Volume:7 Page:167-179
ISSN:1527-8999
Container-title:The Chemical Record
language:en
Short-container-title:Chem. Record

Author:

Taguchi Takeo,Saito Akio,Yanai Hikaru

Publisher

Wiley

Subject

Materials Chemistry,General Chemical Engineering,Biochemistry,General Chemistry

Reference38 articles.

1. Styryl Lactones and Their Derivatives: Biological Activities, Mechanisms of Action and Potential Leads for Drug Design

2. A Rapid Divergent Synthesis of Highly Substituted δ-Lactones

3. Selenium-Catalyzed Halolactonization: Nucleophilic Activation of Electrophilic Halogenating Reagents

4. Metal-catalyzed lactonization reactions with carbonyl insertion, see: ; In Handbook of Organopalladium Chemistry for Organic Synthesis, Vol. 2. Ed. John Wiley & Sons, Inc.: Hoboken, NJ, 2002; p. 2351.

5. Total Synthesis of (−)-Spongidepsin

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