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Synthesis 2005(14): 2341-2344
DOI: 10.1055/s-2005-870025
DOI: 10.1055/s-2005-870025
PAPER
© Georg Thieme Verlag Stuttgart · New YorkConvenient Synthesis of Volatile Streptomyces Lactones
Further Information
Received
20 January 2005
Publication Date:
14 July 2005 (online)
Publication History
Publication Date:
14 July 2005 (online)
Abstract
A convenient three-step synthetic approach towards 3-alkyl-5-methyl-2[5H]furanones is described. The steps involved in the synthesis are domino primary alcohol oxidation-Wittig reaction, acid-catalysed lactonisation and isomerisation. This synthetic approach has been exploited to synthesise four Streptomyces lactones.
Key words
domino reaction - Wittig reaction - isomerisation - lactone - oxidation
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