107683-39-6Relevant articles and documents
Rapid, benign, and additive-free thiolysis of epoxides under ultrasonic/aqueous conditions
Mojtahedi, Mohammad M.,Khalili, Sajad
, p. 431 - 437 (2014/06/10)
An environmentally friendly and efficient procedure is developed for ring opening of various epoxides with thiols under non-thermal conditions. Reactions take place by ultrasonic irradiation of the two reactants suspended in an additive-free aqueous mediu
BiCl3 catalyzed thiolyzation reaction of 1,2-epoxides with diaryl disulfides in the presence of zinc powder and ionic liquid
Khosropour,Khodaei,Ghozati
, p. 2525 - 2531 (2007/10/03)
A new and efficient method has been developed for the regio- and chemoselective synthesis of β-hydroxysulfides with the ring-opening reaction of 1,2-epoxides by diaryl disulfides and zinc powder in the presence of a catalytic amount of BiCl3 in
InCl3-catalyzed highly regioselective ring opening of epoxides with thiols
Yadav,Reddy,Baishya, Gakul
, p. 906 - 907 (2007/10/03)
Epoxides react smoothly with thiols in the presence of 10 mol% InCl3 under very mild conditions to afford the corresponding β-hydroxy sulfides in high yields with high regioselectivity. Similar yields and selectivity are also obtained with cata