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

Sun Lumin; J R Falck

doi:10.1016/S0040-4039(00)89001-2

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

Sun Lumin, J R Falck

Biochemistry

Research output: Contribution to journal › Article

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 language	English (US)
Pages (from-to)	2971-2974
Number of pages	4
Journal	Tetrahedron Letters
Volume	31
Issue number	21
DOIs	https://doi.org/10.1016/S0040-4039(00)89001-2
State	Published - 1990

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)89001-2

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Lumin, S., & Falck, J. R. (1990). Synthesis and stereochemical revision of a bioactive dihydroxyeicosanoid isolated from the red marine alga farlowia mollis. Tetrahedron Letters, 31(21), 2971-2974. https://doi.org/10.1016/S0040-4039(00)89001-2

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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.",

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AU - Falck, J R

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