Total synthesis of (−)-baconipyrone C

Yadav, J. S. ; Sathaiah, K. ; Srinivas, R. (2009) Total synthesis of (−)-baconipyrone C Tetrahedron, 65 (17). pp. 3545-3552. ISSN 0040-4020

Full text not available from this repository.

Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/j.tet.2008.12.049

Abstract

A highly stereoselective asymmetric total synthesis of marine polypropionate (−)-baconipyrone C has been achieved. Utilization of desymmetrization technique to create five stereogenic centres, Sharpless epoxidation, Gilman's reaction and resolution of methyl group using enzyme PS-C is the highlight of the synthesis.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:(−)-Baconipyrone C; Desymmetrization; Enzymatic Resolution; Sharpless Epoxidation; Gilmans' Reaction
ID Code:58868
Deposited On:02 Sep 2011 03:33
Last Modified:02 Sep 2011 03:33

Repository Staff Only: item control page