200803-17-4Relevant articles and documents
Transition-Metal-Free Stereospecific Oxidative Annulative Coupling of Indolines with Aziridines
Karjee, Pallab,Sarkar, Tanumay,Kar, Subhradeep,Punniyamurthy, Tharmalingam
, p. 8261 - 8270 (2020/07/25)
Tandem C-N bond formation for the oxidative annulation of indolines with aziridines is accomplished employing the combination of DDQ and NaOCl at ambient conditions. Optically active aziridine can be coupled with high enantiomeric purity (>99% ee). The substrate scope, stereocontrol with the enantioenriched substrate, and scale-up are the important practical advantages.
Copper iodide-catalyzed aziridination of alkenes with sulfonamides and sulfamate esters
Chang, Joyce Wei Wei,Ton, Thi My Uyen,Zhang, Zhengyang,Xu, Yanjun,Chan, Philip Wai Hong
scheme or table, p. 161 - 164 (2009/04/14)
An efficient copper iodide-catalyzed aziridination of a variety of alkenes with sulfonamides and sulfamate esters as the nitrogen source and iodosylbenzene (PhI{double bond, long}O) as the oxidant is reported herein. The reaction is operationally straight
Efficient Aziridination of Olefins Catalyzed by a Unique Disilver(I) Compound
Cui, Yong,He, Chuan
, p. 16202 - 16203 (2007/10/03)
A unique disilver(I) compound is an efficient catalyst for aziridination of olefins. Copyright