Reductive Cleavage of S–S Bond by Zn/AlCl<sub>3</sub> System: A Novel Method for the Synthesis of Sulfides from Alkyl Tosylates and Disulfides
作者:Barahman Movassagh、Amir Mossadegh
DOI:10.1081/scc-120039486
日期:2004.1.1
Abstract 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.
Reductive Cleavage of the S–Si Bond in Arylsulfanyltrimethylsilanes: a Novel Method for the Synthesis of Unsymmetrical Sulfides†
作者:Songlin Zhang、Yongmin M. Zhang
DOI:10.1039/a705190e
日期:——
Arylsulfanyltrimethylsilanes are reduced by samarium diiodide to yield samarium arylthiolates which react with alkyl halides to give unsymmetrical sulfides.
芳硫基三甲基硅烷经二碘化钐还原后生成芳硫酸钐,再与烷基卤化物反应生成不对称硫化物。
Feshin,V.P. et al., Journal of Organic Chemistry USSR (English Translation), 1976, vol. 12, p. 1052 - 1056
作者:Feshin,V.P. et al.
DOI:——
日期:——
SYNTHESIS OF ORGANIC SULFIDES VIA Zn/AlCl<sub>3</sub>SYSTEM IN AQUEOUS MEDIA
作者:M. M. Lakouraj、B. Movassagh、Z. Fadaei
DOI:10.1081/scc-120003615
日期:2002.1
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 65degreesC.
Welzel, Peter; Schmidt, Juergen, Liebigs Annalen der Chemie, 1984, # 12, p. 576 - 585