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Synthesis of amido-spiro[2.2]pentanes via Simmons-Smith cyclopropanation of allenamides.

ABSTRACT: A detailed account of Simmons-Smith cyclopropanations of allenamides en route to amido-spiro[2.2]pentanes is described here. While the diastereoselectivity was low when using unsubstituted allenamides, the reaction is overall efficient and general, representing the most direct synthesis of both chemically and biologically interesting amido-spiro[2.2]pentane systems. With alpha-substituted allenamides, while the diastereoselectivity could be improved significantly based on a series of conformational analyses, both mono- and bis-cyclopropanation products were observed. Consequently, several structurally intriguing amido-methylene cyclopropanes could also be prepared.

SUBMITTER: Lu T

PROVIDER: S-EPMC2829688 | biostudies-literature | 2009 Aug

REPOSITORIES: biostudies-literature

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Synthesis of amido-spiro[2.2]pentanes via Simmons-Smith cyclopropanation of allenamides.

Lu Ting T Hayashi Ryuji R Hsung Richard P RP DeKorver Kyle A KA Lohse Andrew G AG Song Zhenlei Z Tang Yu Y

Organic & biomolecular chemistry 20090619 16

A detailed account of Simmons-Smith cyclopropanations of allenamides en route to amido-spiro[2.2]pentanes is described here. While the diastereoselectivity was low when using unsubstituted allenamides, the reaction is overall efficient and general, representing the most direct synthesis of both chemically and biologically interesting amido-spiro[2.2]pentane systems. With alpha-substituted allenamides, while the diastereoselectivity could be improved significantly based on a series of conformatio ...[more]

PMID: 19641792

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