Asymmetric [2,3]-Wittig Rearrangement Approach to the Formal Synthesis of (+)-Brefeldin A

Katsuhiko Tomooka, Katsuya Ishikawa, Takeshi Nakai

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

An asymmetric synthesis of the 2,4-disubstituted 1-cyclopentanal, a key precursor of brefeldin A, is described which involves as the key step an asymmetric [2,3]-Wittig rearrangement to control both the ring and side chain configurations.

Original languageEnglish
Pages (from-to)901-902
Number of pages2
JournalSynlett
Volume1995
Issue number9
DOIs
Publication statusPublished - Sep 1 1995
Externally publishedYes

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Brefeldin A

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

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Asymmetric [2,3]-Wittig Rearrangement Approach to the Formal Synthesis of (+)-Brefeldin A. / Tomooka, Katsuhiko; Ishikawa, Katsuya; Nakai, Takeshi.

In: Synlett, Vol. 1995, No. 9, 01.09.1995, p. 901-902.

Research output: Contribution to journalArticle

Tomooka, Katsuhiko ; Ishikawa, Katsuya ; Nakai, Takeshi. / Asymmetric [2,3]-Wittig Rearrangement Approach to the Formal Synthesis of (+)-Brefeldin A. In: Synlett. 1995 ; Vol. 1995, No. 9. pp. 901-902.
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