Literature DB >> 20609458

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

Thibault Coursindel1, Audrey Restouin, Georges Dewynter, Jean Martinez, Yves Collette, Isabelle Parrot.   

Abstract

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 anti-proliferative activity on breast cancer cells. 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20609458     DOI: 10.1016/j.bioorg.2010.05.002

Source DB:  PubMed          Journal:  Bioorg Chem        ISSN: 0045-2068            Impact factor:   5.275


  2 in total

1.  Cyclic dipeptides produced by fungus Eupenicillium brefeldianum HMP-F96 induced extracellular alkalinization and H2O 2 production in tobacco cell suspensions.

Authors:  Xiaoqi Chen; Yanhua Mou; Junhong Ling; Nan Wang; Xiao Wang; Jiangchun Hu
Journal:  World J Microbiol Biotechnol       Date:  2014-10-25       Impact factor: 3.312

2.  Palladium-Catalyzed Modular Synthesis of Substituted Piperazines and Related Nitrogen Heterocycles.

Authors:  Thomas D Montgomery; Viresh H Rawal
Journal:  Org Lett       Date:  2016-01-29       Impact factor: 6.005

  2 in total

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