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 journalArticle

124 Citations (Scopus)

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 languageEnglish (US)
Pages (from-to)11752-11753
Number of pages2
JournalJournal of the American Chemical Society
Volume128
Issue number36
DOIs
StatePublished - Sep 13 2006

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Palladium
Biological Products
Kinetics
amurensinine

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

A convergent and enantioselective synthesis of (+)-amurensinine via selective C-H and C-C bond insertion reactions. / Tambar, Uttam K.; Ebner, David C.; Stoltz, Brian M.

In: Journal of the American Chemical Society, Vol. 128, No. 36, 13.09.2006, p. 11752-11753.

Research output: Contribution to journalArticle

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