66918-44-3Relevant academic research and scientific papers
Highly regioselective double hydrothiolation of terminal acetylenes with thiols catalyzed by palladium diacetate
Mitamura, Takenori,Daitou, Masayuki,Nomoto, Akihiro,Ogawa, Akiya
scheme or table, p. 413 - 415 (2011/05/16)
Treatment of terminal acetylenes 1 with two equivalents of thiols 2 in the presence of Pd(OAc)2 catalyst and H2O causes regioselective double hydrothiolation of 1, leading to the corresponding dithioketals 3 in moderate to good yields.
Hydrothiolation of unactivated alkynes catalyzed by indium(III) bromide
Yadav,Reddy, B. V. Subba,Raju,Ravindar,Baishya, Gakul
, p. 1474 - 1475 (2008/03/14)
Indium(III) bromide is found to catalyze efficiently the hydrothiolation of unactivated alkynes with various thiols under mild conditions to produce the corresponding dithioacetals in excellent yields. However, addition of aromatic thiols on aromatic alky
A Simple and Convenient Method for the Cleavage of Dithioacetals to the Corresponding Carbonyl Compounds
Cossy, J.
, p. 1113 - 1115 (2007/10/02)
Carbonyl compounds were regenerated in high yields when corresponding diphenyl and diethyl dithioacetals were treated with a mixture of m-chloroperoxybenzoic acid/trifluoroacetic acid in dichloromethane.
