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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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Bibliographic Details
Published in:Synlett 2011-06, Vol.2011 (10), p.1459-1461
Main Authors: Inai, Makoto, Nishii, Takeshi, Mukoujima, Shingo, Esumi, Tomoyuki, Kaku, Hiroto, Tominaga, Keiko, Abe, Hiroaki, Horikawa, Mitsuyo, Tsunoda, Tetsuto
Format: Article
Language:English
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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.
ISSN:0936-5214
1437-2096
DOI:10.1055/s-0030-1260762