Stereospecific total synthesis of somocystinamide A.

Org Lett

Scripps Institution of Oceanography and Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California at San Diego, 9500 Gilman Drive, La Jolla, California 92093, USA.

Published: October 2008

The first total synthesis of somocystinamide A, a disulfide dimer with extremely labile enamide functional groups, was accomplished in a concise and stereospecific manner. Somocystinamide A is reported to possess exceptionally potent antiangiogenic and tumoricidal activities. The current work should enable further pharmacological investigation of this important natural product.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227555PMC
http://dx.doi.org/10.1021/ol8016947DOI Listing

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