64274-23-3Relevant academic research and scientific papers
Zinc chloride catalyzed ring opening of N-arylsulfonyl aziridines by thioamides: A new approach to the synthesis of amidines
Hajibabaei, Khadijeh,Zali-Boeini, Hassan
, p. 2044 - 2048 (2014/11/08)
The first zinc chloride catalyzed ring opening of N-arylsulfonyl aziridines by thioamides is described. Various thioamides were reacted with N-arylsulfonyl aziridines in the presence of a catalytic amount of dry zinc chloride to provide the corresponding
Facile synthesis of sulfonyl amidines and β-amino sulfonyl enamines under transition-metal-free conditions
Gao, Tingting,Zhao, Mingming,Meng, Xu,Li, Chuanbin,Chen, Baohua
experimental part, p. 1281 - 1284 (2011/08/03)
Treatment of enamine and azide resulted in the formation of either sulfonyl amidine or β-amino sulfonyl enamine derivative in moderate to good yields. The reaction could proceed under catalyst-free conditions. Georg Thieme Verlag Stuttgart · New York.
