39504-39-7Relevant articles and documents
Biodegradable choline hydroxide promoted environmentally benign thiolysis of epoxides
Azizi, Najmedin,Edrisi, Mahtab
supporting information, p. 525 - 528 (2016/01/20)
An environmentally benign and rapid thiolysis of epoxides using a biodegradable, choline-based task-specific ionic liquid has been developed. The ring opening reaction of aryl and alkyl epoxides proceeded rapidly and afforded the corresponding β-hydroxysulfides in high yields with excellent regioselectivity. The protocol has the advantages of easy work-up, short reaction times, high yields, and a biodegradable catalyst.
Recyclable superparamagnetic Fe3O4 nanoparticles for efficient catalysis of thiolysis of epoxides
Mojtahedi, Mohammad M.,Abaee, M. Saeed,Rajabi, Azam,Mahmoodi, Peyman,Bagherpoor, Saeed
experimental part, p. 68 - 71 (2012/08/07)
An efficient and rapid procedure is developed for room-temperature ring opening of various epoxides with thiols under solvent-free conditions in the presence of catalytic amount of superparamagnetic Fe3O4 nanoparticles. As a result,
Additive-free thiolysis of epoxides in water: A green and efficient regioselective pathway to β-hydroxy sulfides
Abaee, Saeed M.,Mojtahedi, Mohammad M.,Abbasi, Hassan,Fatemi, Ensieh R.
, p. 282 - 289 (2008/03/17)
Room-temperature ring opening of various epoxides with aromatic thiols was carried out in water in the absence of any Lewis acid or additive. High yields of β-hydroxy sulfides with excellent regioselectivity were obtained under very environmentally friend