28324-32-5Relevant articles and documents
A simple, efficient, and green procedure for the 1,4-addition of thiols to conjugated alkenes and alkynes catalyzed by sodium acetate in aqueous medium
Ranu, Brindaban C.,Mandal, Tanmay
, p. 223 - 227 (2008/02/10)
A benign and inexpensive salt, sodium acetate, efficiently catalyzes 1,4-addition of thiols to a variety of conjugated alkenes such as ?,?-unsaturated ketones, aldehydes, carboxylic esters, nitriles, nitro compounds, and chalcones in aqueous THF. The reac
Formation of zinc thiolates by reductive cleavage of disulfides with the Zn/AlCl3 system in aqueous media, and their use for Michael addition
Movassagh, Barahman,Zakinezhad, Yousef
, p. 47 - 49 (2008/02/10)
A simple, convenient, and efficient one-pot protocol for the reductive cleavage of disulfides and Michael addition to α,β-unsaturated carbonyl compounds mediated by the Zn/AlCl3 system in aqueous media is reported.
Catalysis by ionic liquid: A simple, green and efficient procedure for the Michael addition of thiols and thiophosphate to conjugated alkenes in ionic liquid, [pmIm]Br
Ranu, Brindaban C.,Dey, Suvendu S.
, p. 4183 - 4188 (2007/10/03)
A room temperature ionic liquid, 1-pentyl-3-methylimidazolium bromide, [pmIm]Br efficiently catalyzes Michael addition of thiols and diethyl dithiophosphate to a variety of conjugated alkenes such as α,β- unsaturated carbonyl compounds, carboxylic esters,
