Regioselective synthesis and antimicrobial screening of novel ketocarbazolodispiropyrrolidine derivatives

被引:64
|
作者
Periyasami, Govindasami [1 ]
Raghunathan, Raghavachary [1 ]
Surendiran, Gangadharan [2 ]
Mathivanan, Narayanasamy [2 ]
机构
[1] Univ Madras, Dept Organ Chem, Madras 600025, Tamil Nadu, India
[2] Univ Madras, Ctr Adv Studies Bot, Madras 600025, Tamil Nadu, India
关键词
Keto-carbazole; Azomethine ylides; Cycloaddition; Dispiropyrrolidine; Bioactivity; HYACINTHOIDES-NON-SCRIPTA; PYRROLIZIDINE ALKALOIDS; PYRROLIDINE;
D O I
10.1016/j.ejmech.2008.07.009
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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.
引用
收藏
页码:959 / 966
页数:8
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