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-Reference-Cited by-同舟云学术

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

Published:1988 Issue:37 Volume:29 Page:4763-4766
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kuroda Satoru,Sakaguchi Shin-ichi,Ikegami Satoru,Hanamoto Takeshi,Katsuki Tsutomu,Yamaguchi Masaru

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference5 articles.

1. [2,3]Wittig rearrangement of 2′-alkenyloxyacetic acid esters

2. Construction of four consecutive asymmetric centers I. - and - selective epoxydation of β-methyl--homoallylic alcohols

3. Construction of four consecutive asymmetric centers II. Regioselectiveepoxide-ring opening of γ,δ--epoxy-β-methyl alcohols by alkylation

4. 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

5. S. Ikegami, T. Katsuki, and M. Yamaguchi, the succeeding communication.

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