Issue 5, 2015

Structure elucidation of nigricanoside A through enantioselective total synthesis

Abstract

Nigricanoside A was isolated from green alga, and its dimethyl ester was found to display potent cytotoxicity. Its scarcity prevented a full structure elucidation, leaving total synthesis as the only means to determine its relative and absolute stereochemistry and to explore its biological activity. Here we assign the stereochemistry of the natural product through enantioselective total synthesis and provide initial studies of its cytotoxicity.

Graphical abstract: Structure elucidation of nigricanoside A through enantioselective total synthesis

Supplementary files

Article information

Article type
Edge Article
Submitted
24 Jan 2015
Accepted
12 Mar 2015
First published
12 Mar 2015
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2015,6, 2932-2937

Author version available

Structure elucidation of nigricanoside A through enantioselective total synthesis

J. Chen, P. Koswatta, J. R. DeBergh, P. Fu, E. Pan, J. B. MacMillan and J. M. Ready, Chem. Sci., 2015, 6, 2932 DOI: 10.1039/C5SC00281H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements