Stereoselective formal total synthesis of the cyclodepsipeptide (-)-spongidepsin

dc.contributor.author	Chandrasekhar, Srivari
dc.contributor.author	Yaragorla, Srinivasa Rao
dc.contributor.author	Sreelakshmi, Lella
dc.date.accessioned	2022-03-27T08:50:33Z
dc.date.available	2022-03-27T08:50:33Z
dc.date.issued	2007-10-08
dc.description.abstract	The formal total synthesis of (-)-spongidepsin is achieved starting from easily available raw materials involving asymmetric α-hydroxylation, Enders alkylation, and RCM as key reactions. © 2007 Elsevier Ltd. All rights reserved.
dc.identifier.citation	Tetrahedron Letters. v.48(41)
dc.identifier.issn	00404039
dc.identifier.uri	10.1016/j.tetlet.2007.08.017
dc.identifier.uri	https://www.sciencedirect.com/science/article/abs/pii/S0040403907015961
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/11917
dc.subject	(-)-Citronellol
dc.subject	d-Proline
dc.subject	Enders auxillary
dc.subject	Phenyl alanine
dc.subject	RCM
dc.subject	Roche ester
dc.subject	Yamaguchi esterification
dc.title	Stereoselective formal total synthesis of the cyclodepsipeptide (-)-spongidepsin
dc.type	Journal. Article
dspace.entity.type

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