Issue 5, 2014

New facile enantio- and diastereo-selective syntheses of (−)-triptonide and (−)-triptolide

Abstract

A novel formal asymmetric synthesis of (−)-triptonide and (−)-triptolide, featuring a new alternative access to their known key intermediate 4, has been achieved through two synthetic routes in 9 steps with 13.6% total yield and 10 steps with 18.5% overall yield, respectively. This synthesis is scalable and hence has high potential for application to further synthetic elaboration and biologic investigation on such natural products.

Graphical abstract: New facile enantio- and diastereo-selective syntheses of (−)-triptonide and (−)-triptolide

Supplementary files

Article information

Article type
Communication
Submitted
04 Nov 2013
Accepted
29 Nov 2013
First published
02 Dec 2013

Org. Biomol. Chem., 2014,12, 732-736

New facile enantio- and diastereo-selective syntheses of (−)-triptonide and (−)-triptolide

H. Zhang, H. Li, J. Xue, R. Chen, Y. Li, Y. Tang and C. Li, Org. Biomol. Chem., 2014, 12, 732 DOI: 10.1039/C3OB42183J

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