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A Convergent and Enantioselective Synthesis of (+)-Amurensinine via Selective C–H and C–C Bond Insertion Reactions

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 lab...

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Detalhes bibliográficos
Main Authors: Tambar, Uttam K., Ebner, David C., Stoltz, Brian M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2006
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2529249/
https://ncbi.nlm.nih.gov/pubmed/16953603
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ja0651815
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