4.5 Article

Stereoselective synthesis of the macrocyclic core of (-)-salicylihalamides A and B

Journal

SYNTHESIS-STUTTGART
Volume -, Issue 7, Pages 1070-1076

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-2007-965970

Keywords

salicylihalamide; cytotoxicity; Sharpless epoxidation; metathesis

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Stereoselective synthesis of the macrocyclic core of salicylihalamides A and B is described. The synthetic strategy features stereoselective iodolactonization, Sharpless asymmetric epoxidation, Mitsunobu esterification, and ring-closing metathesis.

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