Convenient synthesis of volatile Streptomyces lactones

Amonkar, C.P.; Tilve, S.G.; Parameswaran, P.S.

dc.contributor.author	Amonkar, C.P.
dc.contributor.author	Tilve, S.G.
dc.contributor.author	Parameswaran, P.S.
dc.date.accessioned	2015-06-03T08:28:02Z
dc.date.available	2015-06-03T08:28:02Z
dc.date.issued	2005
dc.identifier.citation	Synthesis-Stuttgart. (14); 2005; 2341-2344.	en_US
dc.identifier.uri	http://dx.doi.org/10.1055/s-2005-870025
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/1710
dc.description.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.	en_US
dc.publisher	Thieme Publishing	en_US
dc.subject	Chemistry	en_US
dc.title	Convenient synthesis of volatile Streptomyces lactones	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y