Reductive Cleavage of S–S Bond by Zn/AlCl3 System: A Novel Method for the Synthesis of Sulfides from Alkyl Tosylates and Disulfides
B Movassagh, A Mossadegh
Index: Movassagh; Lakouraj; Fadaei Journal of Chemical Research - Part S, 2000 , # 7 p. 350 - 351
Full Text: HTML
Citation Number: 15
Abstract
Alkyl and aryl disulfides are reduced by zinc powder in the presence of AlCl 3 in aqueous media to yield zinc thiolates. These thiolate anion species then react with alkyl tosylates to give sulfides in high to excellent yields. ... Alkyl and aryl disulfides are reduced by zinc powder in the presence
Related Articles:
Eigenschaften eines (Arylthiomethylen) cyclohexanons
[Welzel, Peter; Schmidt, Juergen Liebigs Annalen der Chemie, 1984 , # 12 p. 576 - 585]
Eigenschaften eines (Arylthiomethylen) cyclohexanons
[Welzel, Peter; Schmidt, Juergen Liebigs Annalen der Chemie, 1984 , # 12 p. 576 - 585]