55181-35-6Relevant articles and documents
Catalyst-free chemoselective α-sulfenylation/β-thiolation for α,β-unsaturated carbonyl compounds
Huang, Xi,Li, Juan,Li, Xiang,Wang, Jiayi,Peng, Yanqing,Song, Gonghua
, p. 26419 - 26424 (2019/09/13)
A novel, efficient, catalyst-free and product-controllable strategy has been developed for the chemoselective α-sulfenylation/β-thiolation of α,β-unsaturated carbonyl compounds. An aromatic sulfur group could be chemoselectively introduced at α-or β-posit
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,
Oxidative Desulfenylation of β-Alkylthio- and β-Arylthio-aldehydes and -ketones to α,β-Unsaturated Carbonyl Compounds
Nishio, Takehiko,Omote, Yoshimori
, p. 392 - 394 (2007/10/02)
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