Synthesis of highly substituted cyclopentenones via the [4 + 1] cycloaddition of nucleophilic carbenes and vinyl ketenes

James H. Rigby; Zhengqiang Wang

doi:10.1021/ol0272141

Synthesis of highly substituted cyclopentenones via the [4 + 1] cycloaddition of nucleophilic carbenes and vinyl ketenes

James H. Rigby, Zhengqiang Wang

Research output: Contribution to journal › Article › peer-review

61 Scopus citations

Abstract

(Matrix presented) Vinyl ketenes have been shown to undergo [4 + 1] cycloaddition with a variety of nucleophilic carbenes to deliver highly substituted cyclopentenones as products.

Original language	English (US)
Pages (from-to)	263-264
Number of pages	2
Journal	Organic Letters
Volume	5
Issue number	3
DOIs	https://doi.org/10.1021/ol0272141
State	Published - Feb 6 2003
Externally published	Yes

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title = "Synthesis of highly substituted cyclopentenones via the [4 + 1] cycloaddition of nucleophilic carbenes and vinyl ketenes",

abstract = "(Matrix presented) Vinyl ketenes have been shown to undergo [4 + 1] cycloaddition with a variety of nucleophilic carbenes to deliver highly substituted cyclopentenones as products.",

author = "Rigby, {James H.} and Zhengqiang Wang",

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journal = "Organic Letters",

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AU - Rigby, James H.

AU - Wang, Zhengqiang

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N2 - (Matrix presented) Vinyl ketenes have been shown to undergo [4 + 1] cycloaddition with a variety of nucleophilic carbenes to deliver highly substituted cyclopentenones as products.

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JO - Organic Letters

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Synthesis of highly substituted cyclopentenones via the [4 + 1] cycloaddition of nucleophilic carbenes and vinyl ketenes

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