4.7 Article

Regioselective synthesis and antimicrobial screening of novel ketocarbazolodispiropyrrolidine derivatives

期刊

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
卷 44, 期 3, 页码 959-966

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2008.07.009

关键词

Keto-carbazole; Azomethine ylides; Cycloaddition; Dispiropyrrolidine; Bioactivity

资金

  1. Department of Science and Technology (DST), New Delhi, India

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A series of novel dispiropyrrolidine derivatives have been synthesized through 1,3-dipolar cycloaddition reaction of azomethine ylide generated from sarrosin and di/tri ketone with the dipolarophile (E)-2-arylidine-1-keto-carbazoles. The cycloadducts ketocarbazalo spiro N-methyl pyrrolidines showed the most interesting antimicrobial activity at lower concentration. (C) 2008 Elsevier Masson SAS. All rights reserved.

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