Stereoselective Synthesis of the Monomeric Unit of Actin Binding Macrolide Rhizopodin

Pulukuri, K K; Chakraborty, Tushar Kanti

dc.contributor.author	Pulukuri, K K
dc.contributor.author	Chakraborty, Tushar Kanti
dc.date.accessioned	2012-11-19T09:26:50Z
dc.date.available	2012-11-19T09:26:50Z
dc.date.issued	2012
dc.identifier.citation	Organic Letter, 2012, 14 (11), 2858–2861	en
dc.identifier.uri	http://hdl.handle.net/123456789/981
dc.description.abstract	An efficient, scalable and stereocontrolled synthesis of the entire carbon framework of an actin binding dimeric macrolide rhizopodin has been accomplished in its protected form. The key features of our synthesis include a titanium catalyzed anti acetal aldol reaction, substrate controlled diastereoslelective prenyl stannylation, Mukaiyama aldol reaction, an indium mediated diastereoselective propargylation and an advanced stage Stille coupling reaction.	en
dc.format.extent	339356 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CDRI Communication No. 8250	en
dc.subject	Stereoselective Synthesis	en
dc.subject	Macrolide Rhizopodin	en
dc.title	Stereoselective Synthesis of the Monomeric Unit of Actin Binding Macrolide Rhizopodin	en
dc.type	Article	en