Synthesis of Trisubstituted Alkenes via Olefin Cross-Metathesis-Reference-Cited by-同舟云学术

Synthesis of Trisubstituted Alkenes via Olefin Cross-Metathesis

Published:1999-11-02 Issue:11 Volume:1 Page:1751-1753
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Chatterjee Arnab K.¹,Grubbs Robert H.¹

Affiliation:

1. The Arnold and Mabel Beckman Laboratory of Chemical Synthesis, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol991023p

Reference53 articles.

1. Claisen rearrangement of allyl esters

2. The stereoselective generation of ester enolates

3. The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation

4. A highly stereoselective synthesis of Z-trisubstituted olefins via [2,3]-sigmatropic rearrangement. Preference for a pseudoaxially substituted transition state

5. Preparation and rearrangement of trans-3-(allyloxy)acrylic acids: a Claisen sequence that avoids mercury catalysis

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