A diastereo- and enantioselective Michael addition of chiral amide enolates to α, β-unsaturated esters a stereoelective synthesis of (+)-dehydroiridodiol and (-)-isodehydroiridodiol

Masahiko Yamaguchi, Koichi Hasebe, Shinya Tanaka, Toru Minami

Research output: Contribution to journalArticle

59 Citations (Scopus)

Abstract

(+)-Dehydroiridodiol and (-)-isodehydroiridodiol were synthesized stereoselectively using the diastereo- and enantioselective Michael addition of chiral amide enolates to α, β-unsaturated esters.

Original languageEnglish
Pages (from-to)959-962
Number of pages4
JournalTetrahedron Letters
Volume27
Issue number8
DOIs
Publication statusPublished - 1986 Jan 1
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Fingerprint Dive into the research topics of 'A diastereo- and enantioselective Michael addition of chiral amide enolates to α, β-unsaturated esters a stereoelective synthesis of (+)-dehydroiridodiol and (-)-isodehydroiridodiol'. Together they form a unique fingerprint.

  • Cite this