1296864-16-8Relevant academic research and scientific papers
Cationic micelle-catalyzed ring-opening reactions of aziridines with thiols in water
Yang, Min,Yang, Qin,Chen, Puqing,Peng, Yiyuan
experimental part, p. 499 - 503 (2012/01/05)
An efficient and practical method is described for the ring-opening reactions of N-tosylaziridines with various thiols in water under mild conditions. Various surfactants have been evaluated to optimize the reactions. Under optimal conditions, these react
Pyridine-N-oxide: An efficient organocatalyst for ring-opening reactions of aziridines with aryl thiols
Yang, Qin,Yin, Zhenlan,Yang, Min,Peng, Yiyuan
experimental part, p. 79 - 84 (2012/03/27)
Pyridine-N-oxide serves as an efficient catalyst for the ring-opening reactions of N-tosylaziridines with various aryl thiols under mild conditions. This transformation is highly effective, which gives rise to the corresponding β-amino sulfides in good to
