Concise Total Synthesis and Stereochemical Revision of all (−)-Trigonoliimines
The concise and enantioselective total syntheses of (−)-trigonoliimines A, B, and C are described. Our unified strategy to all three natural products is based on asymmetric oxidation and reorganization of a single bistryptamine, a sequence of transformations with possible biogenetic relevance. We re...
المؤلفون الرئيسيون: | , |
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مؤلفون آخرون: | |
التنسيق: | مقال |
اللغة: | en_US |
منشور في: |
American Chemical Society (ACS)
2013
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الوصول للمادة أونلاين: | http://hdl.handle.net/1721.1/82467 https://orcid.org/0000-0003-3080-1063 |