52772-73-3Relevant academic research and scientific papers
Electrocatalytic Synthesis of gem -Bisarylthio Enamines and α-Phenylthio Ketones via a Radical Process under Mild Conditions
Pan, Yong-Zhou,Cheng, Shi-Yan,Li, Qian-Yu,Tang, Hai-Tao,Pan, Ying-Ming,Meng, Xiu-Jin,Mo, Zu-Yu
supporting information, p. 593 - 600 (2021/03/17)
The novel method for the synthesis of gem -bisarylthio enamines and α-phenylthio ketones was developed via the coupling of α-substituted vinyl azides with thiols in the presence of tetrabutylammonium iodide (TBAI) as a redox catalyst and electrolyte at ro
Substrate-switched dual functionalization of alkenes: Catalyst-free synthetic route for β-hydroxy and β-keto thioethers
Badsara, Satpal Singh,Singh, Pratibha,Choudhary, Rakhee,Bai, Rekha,Sharma, Mahesh C.
supporting information, p. 11045 - 11049 (2019/07/31)
In this study, a substrate-controlled dual functionalization of alkenes under catalyst-free and solvent-free conditions is described. Alkenes possessing different electron-withdrawing groups, namely, ester and nitrile, reacted with a variety of thiols under air to provide β-hydroxy thioethers and β-keto thioethers, respectively, in good to excellent yields.
