[2,3]Wittig rearrangement of 2′-alkenyloxyacetic acid esters-Reference-Cited by-同舟云学术

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

Published:1986 Issue:38 Volume:27 Page:4581-4582
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Uchikawa Masako,Katsuki Tsutomu,Yamaguchi Masaru

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference5 articles.

1. M.Uchikawa, T.Hanamoto, T.Katsuki, and M.Yamaguchi, preceding communication on this issue.

2. The [2,3]Wittig rearrangement of 2-alkenyloxyacetic acids and its applications to the stereocontrolled synthesis of β, γ-unsaturated aldehydes and conjugated dienoic acids

3. The first practical method for asymmetric epoxidation

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

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4. Sigmatropic Rearrangements in Stereoselective Synthesis;Stereoselective Synthesis of Drugs and Natural Products;2013-10-02

5. Cycloadditions and Rearrangements;Principles of Asymmetric Synthesis;2012

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