120915-27-7Relevant articles and documents
Palladium-Catalyzed Regioselective Three-Component Cascade Bisthiolation of Terminal Alkynes
Li, Jianxiao,Li, Can,Ouyang, Lu,Li, Chunsheng,Yang, Shaorong,Wu, Wanqing,Jiang, Huanfeng
, p. 1138 - 1150 (2018)
An efficient and novel NHC(N-heterocyclic carbene)-palladium-catalyzed three-component cascade bisthiolation of terminal alkynes, K2S (potassium sulfide) and diaryliodonium salts for the assembly of functionalized (Z)-1,2-bis(arylthio)alkene derivatives has been accomplished for the first time. This unique observation features a broad substrate scope, excellent functional-group tolerance, and high regioselectivity. Especially, an arylthiolate anion from diaryliodonium salts and potassium sulfide was proposed as the key intermediate in the catalytic cycle. (Figure presented.).
Addition of diaryl disulfides to terminal alkynes catalysed by an MCM-41-supported bidentate phosphine palladium(0) complex
Li, Jianying,Liu, Jun,Cai, Mingzhong
experimental part, p. 616 - 618 (2011/02/26)
A variety of (Z)-1,2-bis(arylthio)-substituted alkenes have been conveniently synthesised in high yields by the stereoselective addition of diaryl disulfides to terminal alkynes catalysed by an MCM-41-supported bidentate phosphine palladium(0) complex. Th
Palladium-catalyzed thioesterirication of alkynes with O-methyl S-phenyl thiocarbonate
Hua,Takeda,Onozawa,Abe,Tanaka
, p. 2899 - 2900 (2007/10/03)
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