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Stereoselective ring contraction of 2,5-diketopiperazines : An innovative approach to the synthesis of promising bioactive 5-membered scaffolds
Journal article   Peer reviewed

Stereoselective ring contraction of 2,5-diketopiperazines : An innovative approach to the synthesis of promising bioactive 5-membered scaffolds

Thilbault Coursindel, Audrey Restouin, Georges Dewynter, Jean Martinez, Yves Collette and Isabelle Parrot
Bioorganic Chemistry, Vol.38, pp.210-217
2010

Abstract

Ring contraction Diketopiperazines Stereoselective rearrangement Spiroheterocycle Anti-proliferative activity
Ring contraction of 2,5-diketopiperazines by TRAL-alkylation led us to the stereoselective synthesis of original pyrrolidine-2,4-diones, a novel series of promising molecules with moderate antiproliferative activity on breast cancer cells.
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