Unexpected synthesis of aziridines under Cu(I) catalyzed Kinugasa conditions assisted by microwave irradiation

被引：5
|
作者：
Abda, Heithem [1 ]
Aouadi, Kaiss [1 ]
Brahmi, Jihed [1 ]
Msaddek, Moncef [1 ]
Vidal, Sebastien [2 ]
机构：
[1] Univ Monastir, Fac Sci Monastir, Lab Synth Heterocycl Prod Nat & React, Ave Environm, Monastir 5000, Tunisia
[2] Univ Lyon, Inst Chim & Biochim Mol & Supramol, UMR CNRS 5246, Lab Chim Organ Glycochim 2, Batiment Curien,43 Blvd 11 Novembre 1918, F-69622 Villeurbanne, France
来源：
COMPTES RENDUS CHIMIE | 2016年 / 19卷 / 03期
关键词：
Nitrone; Alkynes; 1,3-Dipolar cycloaddition; Aziridines; Microwaves; 1,3-DIPOLAR CYCLOADDITION; CHIRAL NITRONES; 4-ISOXAZOLINES; REARRANGEMENT; ALKYNES; ACYLAZIRIDINES; DERIVATIVES; ALKENES;
D O I：
10.1016/j.crci.2015.09.009
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Cu(I)-catalyzed 1,3-dipolar cycloaddition between chiral nitrone and terminal alkynes under microwave irradiation afforded a series of enantiopure aziridines with the creation of two contiguous stereogenic centers. (C) 2015 Academie des sciences. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码：275 / 278
页数：4
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