Synthesis 2007(14): 2198-2202  
DOI: 10.1055/s-2007-983755
PAPER
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Natural Fimbrolides

Kishan P. Haval, Narshinha P. Argade*
Division of Organic Chemistry (Synthesis), National Chemical Laboratory, Pune 411008, India
e-Mail: np.argade@ncl.res.in;
Further Information

Publication History

Received 7 March 2007
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.