Studies directed towards the synthesis rhizopodin: stereoselective synthesis of the C1-C15 fragment

Chakraborty, T K; Pulukuri, K K; Sreekanth, Midde

dc.contributor.author	Chakraborty, T K
dc.contributor.author	Pulukuri, K K
dc.contributor.author	Sreekanth, Midde
dc.date.accessioned	2014-07-21T10:37:41Z
dc.date.available	2014-07-21T10:37:41Z
dc.date.issued	2010
dc.identifier.citation	Tetrahedron Letters 2010, 51(49), 6444 – 6446	en
dc.identifier.uri	http://hdl.handle.net/123456789/1312
dc.description.abstract	A stereoselective synthesis of the C1-C15 fragment of a G-actin binding natural macrodiolide, rhizopodin was achieved using, as key steps, highly stereoselective acetate aldol reactions to build the C1-C7 fragment, one pot oxazole synthesis and an asymmetric Keck allylation reaction to build the C8-C15 fragment and finally, a Stille reaction to couple both the fragments.	en
dc.format.extent	163015 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CSIR-CDRI Communication No. 7964	en
dc.subject	Rhizopodin	en
dc.subject	Acetate aldol reaction	en
dc.subject	Keck allylation	en
dc.subject	Stille coupling	en
dc.title	Studies directed towards the synthesis rhizopodin: stereoselective synthesis of the C1-C15 fragment	en
dc.type	Article	en