One-pot synthesis of aziridines from vinyl selenones and variously functionalized primary amines

被引:35
作者
Sternativo, Silvia [1 ]
Marini, Francesca [1 ]
Del Verme, Francesca [1 ]
Calandriello, Antonella [1 ]
Testaferri, Lorenzo [1 ]
Tiecco, Marcello [1 ]
机构
[1] Univ Perugia, Sez Chim Organ, Dipartimento Chim & Tecnol Farmaco, I-06123 Perugia, Italy
关键词
Aziridine; Vinyl selenone; Aza-Michael reaction; Ring-closure; Water; AZA-MICHAEL ADDITION; MOLECULAR-SIEVES; 4A; STEREOSELECTIVE-SYNTHESIS; EFFICIENT SYNTHESIS; CONJUGATE ADDITION; RATE ACCELERATION; EPOXIDES; ALKENES; AMBERLYST-15; SELENOXIDES;
D O I
10.1016/j.tet.2010.06.055
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Variously substituted aziridines were conveniently prepared by an aza-Michael Initiated Ring Closure (aza-MIRC) reaction starting from vinyl selenones and primary amines, aminoalcohols or diamines. The reactions proceed in very high yields at room temperature in toluene or water. A significant rate acceleration was observed under aqueous conditions. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6851 / 6857
页数:7
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