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

4 Citations (Scopus)

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

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Rhodophyta
Eicosanoids
Military Personnel
Algae

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Synthesis and stereochemical revision of a bioactive dihydroxyeicosanoid isolated from the red marine alga farlowia mollis. / Lumin, Sun; Falck, J R.

In: Tetrahedron Letters, Vol. 31, No. 21, 1990, p. 2971-2974.

Research output: Contribution to journalArticle

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