Volume 31, Issue 51
Natural Products
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ChemInform Abstract: Synthetic Studies on Brevetoxin-B. Part 2. Stereoselective Synthesis of the EFG-Ring System.

Goh Matsuo

Goh Matsuo

Inst. Phys. Chem. Res., RIKEN, Wako, Saitama 351-01, Japan

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Nobuyuki Hori

Nobuyuki Hori

Inst. Phys. Chem. Res., RIKEN, Wako, Saitama 351-01, Japan

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Hiroko Matsukura

Hiroko Matsukura

Inst. Phys. Chem. Res., RIKEN, Wako, Saitama 351-01, Japan

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Tadashi Nakata

Tadashi Nakata

Inst. Phys. Chem. Res., RIKEN, Wako, Saitama 351-01, Japan

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First published: 31 May 2010

Abstract

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ChemInform Abstract

The title compound (X) is synthesized via stepwise construction of the E, F, and G ring using a stereoselective Michael addition of the α-methyl group, a novel ring expansion of compound (V), and 6-endo cyclizations of vinylepoxide (VII) and methylepoxide (IX).

chemical structure image

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