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...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
American Chemical Society (ACS),
2013-11-18T20:37:57Z.
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Subjects: | |
Online Access: | Get fulltext |