A highly stereoselective synthesis of Z-disubstituted olefin by O-assisted Still-Wittig rearrangement-Reference-Cited by-同舟云学术

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A highly stereoselective synthesis of Z-disubstituted olefin by O-assisted Still-Wittig rearrangement

Published:1996-01 Issue:3 Volume:37 Page:389-392
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Fujii Kazushige,Hara Osamu,Fujita Yoko,Sakagami Youji

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference10 articles.

1. [2,3]-Wittig sigmatropic rearrangements in organic synthesis

2. 2,3-Sigmatropic Rearrangements;Bruckner,1991

3. [2,3]Wittig rearrangement of 2′-alkenyloxyacetic acid esters

4. Stereoselectivity in [2,3]wittig rearrangement of isopropyl [(2E)-1 -(ω-benzyloxyalkyl)-2-butenyl]oxyacetate. Preparation of potent building blocks for the synthesis of polyoxo compounds

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

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