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