Peloruside B, a potent antitumor macrolide from the New Zealand marine sponge Mycale hentscheli: isolation, structure, total synthesis, and bioactivity

AJ Singh, CX Xu, X Xu, LM West… - The Journal of …, 2010 - ACS Publications
AJ Singh, CX Xu, X Xu, LM West, A Wilmes, A Chan, E Hamel, JH Miller, PT Northcote
The Journal of organic chemistry, 2010ACS Publications
Peloruside B (2), a natural congener of peloruside A (1), was isolated in sub-milligram
quantities from the New Zealand marine sponge Mycale hentscheli. Peloruside B promotes
microtubule polymerization and arrests cells in the G2/M phase of mitosis similar to
paclitaxel, and its bioactivity was comparable to that of peloruside A. NMR-directed isolation,
structure elucidation, structure confirmation by total synthesis, and bioactivity of peloruside B
are described in this article. The synthesis features Sharpless dihydroxylation, Brown's …
Peloruside B (2), a natural congener of peloruside A (1), was isolated in sub-milligram quantities from the New Zealand marine sponge Mycale hentscheli. Peloruside B promotes microtubule polymerization and arrests cells in the G2/M phase of mitosis similar to paclitaxel, and its bioactivity was comparable to that of peloruside A. NMR-directed isolation, structure elucidation, structure confirmation by total synthesis, and bioactivity of peloruside B are described in this article. The synthesis features Sharpless dihydroxylation, Brown’s asymmetric allylboration reaction, reductive aldol coupling, Yamaguchi macrolactonization, and selective methylation.
ACS Publications
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