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Total Synthesis of (+)-Brefeldin C Utilizing Aza-Claisen Rearrangement
Abstract The total synthesis of (+)-brefeldin C was accomplished. An asymmetric aza-Claisen rearrangement developed by our laboratory was employed to construct the C-4 and C-5 stereogenic centers of (+)-brefeldin C as a key step.
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Published in: | Synlett 2011-06, Vol.2011 (10), p.1459-1461 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Abstract
The total synthesis of (+)-brefeldin C was accomplished. An
asymmetric aza-Claisen rearrangement developed by our laboratory
was employed to construct the C-4 and C-5 stereogenic centers of
(+)-brefeldin C as a key step. |
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ISSN: | 0936-5214 1437-2096 |
DOI: | 10.1055/s-0030-1260762 |