Issue 11, 2014

Towards the diastereoselective synthesis of derivative of 11′-epi-brevipolide H

Abstract

An efficient diastereoselective synthesis of brevipolide H derivative is described. The approach features the use of (i) catalytic asymmetric transfer hydrogenation, (ii) hydroxyl-directed cyclopropanation, and (iii) substrate-controlled catalytic epoxidation and ring-closing metathesis. Remarkably, in this convergent synthesis process, stereogenic centers were installed through catalytic reactions with high stereocontrol, which greatly facilitates the synthesis of stereo-divergent derivatives.

Graphical abstract: Towards the diastereoselective synthesis of derivative of 11′-epi-brevipolide H

Supplementary files

Additions and corrections

Article information

Article type
Paper
Submitted
26 Nov 2013
Accepted
07 Jan 2014
First published
08 Jan 2014

Org. Biomol. Chem., 2014,12, 1793-1803

Towards the diastereoselective synthesis of derivative of 11′-epi-brevipolide H

G. Kumaraswamy, N. Jayaprakash, D. Rambabu, A. Ganguly and R. Banerjee, Org. Biomol. Chem., 2014, 12, 1793 DOI: 10.1039/C3OB42367K

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