A convergent and enantioselective synthesis of (+)-amurensinine via selective C-H and C-C bond insertion reactions

Uttam K. Tambar; David C. Ebner; Brian M. Stoltz

doi:10.1021/ja0651815

A convergent and enantioselective synthesis of (+)-amurensinine via selective C-H and C-C bond insertion reactions

Uttam K. Tambar, David C. Ebner, Brian M. Stoltz

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

148 Scopus citations

Abstract

A convergent and enantioselective synthesis of the natural product amurensinine is described. The synthetic strategy takes advantage of mild and selective C-H and C-C bond insertion reactions, in addition to the palladium-catalyzed aerobic oxidative kinetic resolution recently developed in these laboratories.

Original language	English (US)
Pages (from-to)	11752-11753
Number of pages	2
Journal	Journal of the American Chemical Society
Volume	128
Issue number	36
DOIs	https://doi.org/10.1021/ja0651815
State	Published - Sep 13 2006

ASJC Scopus subject areas

Catalysis
General Chemistry
Biochemistry
Colloid and Surface Chemistry

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10.1021/ja0651815

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title = "A convergent and enantioselective synthesis of (+)-amurensinine via selective C-H and C-C bond insertion reactions",

abstract = "A convergent and enantioselective synthesis of the natural product amurensinine is described. The synthetic strategy takes advantage of mild and selective C-H and C-C bond insertion reactions, in addition to the palladium-catalyzed aerobic oxidative kinetic resolution recently developed in these laboratories.",

author = "Tambar, {Uttam K.} and Ebner, {David C.} and Stoltz, {Brian M.}",

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AU - Tambar, Uttam K.

AU - Ebner, David C.

AU - Stoltz, Brian M.

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Y1 - 2006/9/13

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AB - A convergent and enantioselective synthesis of the natural product amurensinine is described. The synthetic strategy takes advantage of mild and selective C-H and C-C bond insertion reactions, in addition to the palladium-catalyzed aerobic oxidative kinetic resolution recently developed in these laboratories.

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A convergent and enantioselective synthesis of (+)-amurensinine via selective C-H and C-C bond insertion reactions

Abstract

ASJC Scopus subject areas

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