359678-99-2Relevant articles and documents
Quinine-catalyzed enantioselective desymmetrization of meso-aziridines with benzenethiols
Wang, Zhiyong,Sun, Xiaoyu,Ye, Shengqing,Wang, Weizi,Wang, Bing,Wu, Jie
, p. 964 - 969 (2008)
Ring opening of meso-aziridines with benzenethiols utilizing quinine as an organocatalyst has been developed. The reaction proceeded smoothly in the presence of 10 mol % of quinine in CHCl3 to afford β-amino sulfides in high yields and with mod
Bismuth triflate as novel and efficient catalyst for the synthesis of β-aminosulfides
Yadav, Jhillu S.,Reddy, B. V. Subba,Baishya, Gakul,Reddy, P. Venkatram,Harshavardhan
, p. 1854 - 1858 (2004)
Aziridines undergo ring opening readily with various thiols in the presence of 5 mol% bismuth triflate under very mild reaction conditions to afford the corresponding β-aminosulfides in excellent yields with high regioselectivity.
An efficient procedure for cleavage of aziridines with various thiols promoted by ZnCl2
Wu,Hou,Dai
, p. 1314 - 1317 (2007/10/03)
The ring-opening reaction of aziridines with various thiophenols and thiols catalyzed by ZnCl2 provides β-amino sulfides in high yield.