4.4 Article

Use of chiral sulfoxide in the asymmetric synthesis of (+)-virol C

Journal

SYNLETT
Volume -, Issue 8, Pages 1335-1337

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-2002-32973

Keywords

natural products; chiral sulfoxides; total synthesis; copper-coupling; Pummerer reaction

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The total synthesis of virol C 1 was accomplished using a diastereoselective carbonyl reduction induced by a chiral sulfoxide, a Pummerer rearrangement to give the corresponding aldehyde fragment, and coupling reactions using Wittig and Cadiot-Chodkiewicz protocols.

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