NBS-Mediated Aziridination between Styrenes and Amides under Transition Metal-Free Conditions

被引：5
|
作者：
Meng, Xu [1 ]
Chen, Wenlin [1 ]
Zhang, Yuanqing [1 ]
Chen, Yongxin [1 ]
Chen, Baohua [1 ]
机构：
[1] Lanzhou Univ, Key Lab Nonferrous Met Chem & Resources Utilizat, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
来源：
JOURNAL OF HETEROCYCLIC CHEMISTRY | 2014年 / 51卷 / 04期
基金：
美国国家科学基金会;
关键词：
COPPER-CATALYZED AMIDATION; C-H BONDS; EFFICIENT AZIRIDINATION; ATOM-TRANSFER; CHLORAMINE-T; BROMAMINE-T; OLEFINS; COMPLEXES; ALKENES; SULFONAMIDES;
D O I：
10.1002/jhet.1555
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
An efficient and simple protocol for N-bromosuccinimide (NBS)-mediated styrenes aziridination using amides as the nitrenoid source has been developed. This aziridination affords desired products in moderate to good yields without using transition metal catalyst under very mild reaction condition.
引用
收藏
页码：937 / 942
页数：6
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