The Mitsunobu Reaction of 1,2-O-Benzylideneconduritol E: A New Route to Conduritol F

Takehiko Yoshimitsu, Kunio Ogasawara

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

The Mitsunobu reaction of optically active 1,2-O-benzylideneconduritol E with p-nitrobenzoic acid is found to occur with retention at the C-3 center and with inversion at the C-4 center which leads to a new route to optically active conduritol F.

Original languageEnglish
Pages (from-to)257-259
Number of pages3
JournalSynlett
Volume1995
Issue number3
DOIs
Publication statusPublished - Mar 1 1995
Externally publishedYes

Keywords

  • asymmetric dioxylation
  • conduritol E
  • conduritol F
  • enantiocontrolled synthesis
  • Mitsunobu reaction

ASJC Scopus subject areas

  • Organic Chemistry

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