(4S, 5S)- and (4S, 5R)-5-Hydroxy-4-decanolide (1a and 1b), the proposed autoregulators from Strepotomyces Griseus were synthesized from a propargyl alcohol 2 in an overall yield of 30%, employing the Sharpless asymmetric epoxidation as the key step.

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Volume7, Issue5

October 1989

Pages 458-462

The enantioselective synthesis of (4S,5S)- and (4S,5R)-5-hydroxy-4-decanolide, the autoregulators from Strepotomyces griseus

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The enantioselective synthesis of (4S,5S)- and (4S,5R)-5-hydroxy-4-decanolide, the autoregulators from Strepotomyces griseus

Abstract

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