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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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Détails bibliographiques
Auteurs principaux: Tambar, Uttam K., Ebner, David C., Stoltz, Brian M.
Format: Artigo
Langue:Inglês
Publié: 2006
Sujets:
Accès en ligne: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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