99070-98-1Relevant academic research and scientific papers
A Novel Synthesis of Allyl Sulfides by Organosamarium Reagents
Zhan, Zhuangping,Zhang, Yongmin
, p. 148 - 149 (1998)
Organosamarium reagents react with sodium alkyl thiosulfates to afford allyl Sulfides; a reaction mechanism involving organosamarium(II) and Organosamarium (III) intermediates is suggested.
Synthesis of allylic sulfides via cleavage of S-S bonds promoted by zinc metal in DMF
Du, Jingxing,Zheng, Renwei,Li, Xinsheng
, p. 180 - 181 (2007/10/03)
Cleavage of S-S bonds was achieved without any activation or catalysis, with a Zn/DMF system and subsequent treatment with allylic bromide afforded allylic sulfides in good to excellent yields.
A novel method for the synthesis of allylic sulfides from disulfides and allylytterbium bromide
Su,Li,Zhang,Li
, p. 263 - 264 (2007/10/03)
In presence of trace of methyl iodide (Mel), allylytterbium bromide is formed by the reaction of metallic ytterbium and allylic bromide, which reacts with disulfides to give the corresponding allylic sulfides in good yields under mild and neutral conditions.
A novel synthesis of allyl sulfides in aqueous media promoted by indium
Zhan, Zhuangping,Zhang, Yongmin
, p. 493 - 497 (2007/10/03)
Allyl bromides react smoothly with sodium alkyl thiosulfates promoted by indium in aqueous media to give allyl sulfides in moderate to good yields.
The synthesis of allyl sulfides by organosamarium reagent
Yu, Mingxin,Zhang, Yongmin
, p. 2743 - 2748 (2007/10/03)
Organosamarium reagent reacts with disulfides to afford allyl sulfides in THF.
