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A palladium-catalyzed vinylcyclopropane (3+2) cycloaddition approach to the Melodinus alkaloids.

ABSTRACT: A palladium-catalyzed (3+2) cycloaddition of a vinylcyclopropane and a ?-nitrostyrene is employed to rapidly assemble the cyclopentane core of the Melodinus alkaloids. The ABCD ring system of the natural product family is prepared in six steps from commercially available materials.

SUBMITTER: Goldberg AF

PROVIDER: S-EPMC3155617 | biostudies-literature | 2011 Aug

REPOSITORIES: biostudies-literature

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A palladium-catalyzed vinylcyclopropane (3+2) cycloaddition approach to the Melodinus alkaloids.

Goldberg Alexander F G AF Stoltz Brian M BM

Organic letters 20110725 16

A palladium-catalyzed (3+2) cycloaddition of a vinylcyclopropane and a β-nitrostyrene is employed to rapidly assemble the cyclopentane core of the Melodinus alkaloids. The ABCD ring system of the natural product family is prepared in six steps from commercially available materials. ...[more]

PMID: 21786746

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