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Synthesis 2007(14): 2198-2202
DOI: 10.1055/s-2007-983755
DOI: 10.1055/s-2007-983755
PAPER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of Natural Fimbrolides
Further Information
Received
7 March 2007
Publication Date:
03 July 2007 (online)
Publication History
Publication Date:
03 July 2007 (online)
Abstract
Starting from citraconic anhydride, a three-step approach to fimbrolide congener is reported by taking the advantage of a regioselective Grignard reaction with an anhydride, followed by a dehydrative cyclization and double bromination-dehydrobromination sequence. Starting from N-(4-tolyl)maleimide, an eight-step synthesis of two natural fimbrolides is reported with good yields via the synthesis of requisite butylmaleic anhydride, its regioselective Grignard coupling reaction, and a bromination-dehydrobromination pathway.
Key words
butylmaleic anhydride - regioselective Grignard coupling - butenolides - bromination - fimbrolides
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