52809-72-0Relevant articles and documents
[bmim]OH-promoted one-pot, three-component synthesis of β-nitro sulfides in water
Movassagh, Barahman
, p. 1114 - 1117 (2016/07/27)
A task-specific ionic liquid, [bmim]OH, has been found to be a highly efficient catalyst for one-pot, three-component coupling of aryl aldehydes, nitromethane, and thiols for the synthesis of β-nitro sulfides in water. The main advantages of the present p
Green procedure for the synthesis of β-nitro sulfides by Michael addition of thiols to nitroolefins
Hui, Xin-Ping,Yin, Chao,Ma, Jun,Xu, Peng-Fei
experimental part, p. 676 - 690 (2009/07/18)
Michael addition of thiols to nitroolefins was carried out in water at room temperature without any catalyst, and β-nitro sulfides were obtained in excellent yields. This is the first example of Michael addition of thiols to nitroolefins in water without
Synthesis of aza-Henry products and enamines in water by Michael addition of amines or thiols to activated unsaturated compounds
Ziyaei-Halimehjani, Azim,Saidi, Mohammad R.
, p. 1244 - 1248 (2008/09/17)
Nitroamines and nitrothiols were synthesized in high yields by the Michael addition of amines and thiols to nitroolefins without using any catalyst. Also, the reaction of amines with dimethylacetylene dicarboxylate (DMAD) in water afforded the corresponding enamines.