76475-12-2Relevant articles and documents
Highly efficient regioselective ring openings of N-tosylaziridines to haloamines using ferric (III) halides
Li, Xing,Sun, Zhi-Qin,Chang, Hong-Hong,Wei, Wen-Long
, p. 1174 - 1178 (2014/08/18)
FeX3 (X = Cl, Br) were found to be very effective reagents and powerful catalysts for regioselective ring openings of a variety of N-tosylaziridines with them to afford the corresponding β-haloamines in good to excellent yields with high regios
TBD-catalyzed ring opening of aziridines with silylated nucleophiles
Matsukawa, S.,Takahashi, H.,Harada, T.
, p. 406 - 414,9 (2020/10/15)
The ring opening of N-tosylaziridines with silylated nucleophiles catalyzed by 1,5,7-triazabicyclo[4,4,0]dec-5-ene (TBD) afforded the corresponding- functionalized sulfonamides in excellent yields under mild reaction conditions. Copyright
Polystyrene-supported TBD catalyzed ring-opening of N-tosylaziridines with silylated nucleophiles
Matsukawa, Satoru,Harada, Takeru,Yasuda, Shiori
supporting information; experimental part, p. 4886 - 4890 (2012/07/27)
Polystyrene-supported TBD (PS-TBD) catalyzes the ring-opening of N-tosylaziridines with silylated nucleophiles to give the corresponding products in high yields. PS-TBD was easily recovered and reused without significant loss of catalytic activity.