41932-39-2Relevant academic research and scientific papers
Palladium-Catalyzed Thiocarbonylation of Benzyl Chlorides with Sulfonyl Chlorides for the Synthesis of Arylacetyl Thioesters
Wang, Wei,Qi, Xinxin,Wu, Xiao-Feng
supporting information, p. 2541 - 2545 (2021/03/16)
A convenient procedure for the synthesis of thioesters has been developed via a palladium-catalyzed thiocarbonylation of benzyl chlorides with sulfonyl chlorides. Various arylacetyl thioesters were produced in good yields by using sulfonyl chlorides as an odorless sulfur source. Furthermore, W(CO)6 exhibited dual roles as both a solid CO surrogate and reductant here. (Figure presented.).
Kinetics and mechanism of the aminolysis of aryl phenyldithioacetates in acetonitrile
Oh, Hyuck Keun,Kim, Sun Kyung,Cho, In Ho,Lee, Hai Whang,Lee, Ikchoon
, p. 2306 - 2310 (2007/10/03)
The aminolysis reactions of Z-aryl phenyldithioacetates (C6H5CH2C(=S)SC6H4Z) with benzylamines (XC6H4CH2NH2) are investigated in acetonitrile at -25.0 °C. T
