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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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| Main Authors: | , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2006
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| Teme: | |
| Online dostop: | 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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