Synthesis and stereochemical revision of a bioactive dihydroxyeicosanoid isolated from the red marine alga farlowia mollis

Sun Lumin, J R Falck

Research output: Contribution to journalArticle

5 Scopus citations

Abstract

Chiral trans-enals derived from 2-deoxypyranoses by ylide-induced β-elimination were exploited for the synthesis and stereochemical revision of a novel, marine eicosanoid.

Original languageEnglish (US)
Pages (from-to)2971-2974
Number of pages4
JournalTetrahedron Letters
Volume31
Issue number21
DOIs
StatePublished - 1990

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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