59693-91-3Relevant articles and documents
Reductive cleavage of S-S bond by Zn/AlCl3 system: A novel method for the synthesis of sulfides from alkyl tosylates and disulfides
Movassagh, Barahman,Mossadegh, Amir
, p. 2337 - 2343 (2007/10/03)
Alkyl and aryl disulfides are reduced by zinc powder in the presence of AlCl3 in aqueous media to yield zinc thiolates. These thiolate anion species then react with alkyl tosylates to give sulfides in high to excellent yields.
Synthesis of organic sulfides via Zn/AlCl3 system in aqueous media
Lakouraj,Movassagh,Fadaei
, p. 1237 - 1242 (2007/10/03)
An efficient procedure for preparation of various sulfides has been introduced through a simple reaction of disulfides with suitable alkyl or aryl halides which is promoted by commercial zinc powder in the presence of AlCl3 in aqueous media at 65°C.
Reductive Cleavage of the S-Si Bond in Arylsulfanyltrimethylsilanes: A Novel Method for the Synthesis of Unsymmetrical Sulfides
Zhang, Songtin,Zhang, Yongmin M.
, p. 48 - 49 (2007/10/03)
Arylsulfanyltrimethylsilanes are reduced by samarium diiodide to yield samarium arylthiolates which react with alkyl halides to give unsymmetrical sulfides.