SYNTHESIS AND STEREOCHEMICAL REVISION OF A BIOACTIVE DIHYDROXYEICOSANOID ISOLATED FROM THE RED MARINE ALGA FARLOWIA MOLLIS

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

Source and publish data:

Tetrahedron Letters p. 2971 - 2974 (1990)

Update date:2022-07-29

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Authors:

Lumin, Sun

Falck, J. R.

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Article abstract of DOI:10.1016/S0040-4039(00)89001-2

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.

Full text of DOI:10.1016/S0040-4039(00)89001-2

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