Stereoselective synthesis of the C79–C97 fragment of symbiodinolide
2013 ◽
Vol 9
◽
pp. 1931-1935
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Keyword(s):
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.
Stereoselective synthesis of a marine natural product, (±)-6β-isovaleroxylabda-8,13-diene-7α,15-diol
1996 ◽
Vol 37
(39)
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pp. 7071-7074
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2013 ◽
Vol 13
(10)
◽
pp. 1514-1530
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Keyword(s):