Stereoselective synthesis of C-9 to C-14 segment, a key intermediate for the total synthesis of trienomycin and micotrienins

Yadav, J. S. ; Praveen Kumar, T. K. ; Maniyan, P. P. (1993) Stereoselective synthesis of C-9 to C-14 segment, a key intermediate for the total synthesis of trienomycin and micotrienins Tetrahedron Letters, 34 (18). pp. 2965-2968. ISSN 0040-4039

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

Related URL: http://dx.doi.org/10.1016/S0040-4039(00)60494-X

Abstract

The C-9 to C-14 segment, a key intermediate for the total synthesis of Trienomycin and Micotrienins has been synthesized, involving Sharpless asymmetric epoxidation intramolecular radical cyclisation and MoOPH hydroxylation as key steps.

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ID Code:59554
Deposited On:07 Sep 2011 05:24
Last Modified:07 Sep 2011 05:24

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