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Total synthesis of desacetylumuravumbolide, umuravumbolide and their biological evaluation†
Gowravaram Sabitha,Dodda Vasudeva Reddy,Singam Siva Sankara Reddy,Jhillu. S. Yadav,C. Ganesh Kumar,Pombala Sujitha
RSC Advances Pub Date : 07/11/2012 00:00:00 , DOI:10.1039/C2RA20830J
Abstract

Stereoselective synthesis of naturally occurring α,β-unsaturated lactones desacetylumuravumbolide and umuravumbolide is described. Commercially available propargyl alcohol was used as the starting material. The key steps of this synthesis were alkynylation, a Noyori asymmetric reduction and Still–Gennari olefination. Additionally, the biological activity of umuravumbolides was evaluated on HeLa, MDA-MB-231, MCF7 and A549 cancer cell lines. Umuravumbolide (2) showed potent anticancer activity.

Graphical abstract: Total synthesis of desacetylumuravumbolide, umuravumbolide and their biological evaluation
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