Stereoselective synthesis of the C79-C97 fragment of symbiodinolide

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Abstract

Symbiodinolide is a polyol marine natural product with a molecular weight of 2860. Herein, a streamlined synthesis of the C79-C97 fragment of symbiodinolide is described. In the synthetic route, a spiroacetalization, a Julia-Kocienski olefination, and a Sharpless asymmetric dihydroxylation were utilized as the key transformations. © 2013 Takamura et al.

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Takamura, H., Fujiwara, T., Kadota, I., & Uemura, D. (2013). Stereoselective synthesis of the C79-C97 fragment of symbiodinolide. Beilstein Journal of Organic Chemistry, 9, 1931–1935. https://doi.org/10.3762/bjoc.9.228

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