6263-63-4Relevant academic research and scientific papers
Lewis acid-catalyzed reduction of dithioacetals by 1,4-cyclohexadiene
Ikeshita, Kei-ichiro,Kihara, Nobuhiro,Sonoda, Motohiro,Ogawa, Akiya
, p. 3025 - 3028 (2007)
Dithioacetals were reduced by 1,4-cyclohexadiene in the presence of a catalytic amount of Lewis acid to afford the corresponding sulfides in good yields.
Indium-catalyzed reductive three-component coupling reaction of aliphatic/aromatic carboxylic acids with t-butyl mercaptan leading to unsymmetrical dialkyl sulfides
Sakai, Norio,Yoshimoto, Shunsuke,Miyazaki, Takahiro,Ogiwara, Yohei
supporting information, p. 3117 - 3120 (2016/07/06)
An InI3–TMDS (1,1,3,3-tetramethyldisiloxane) reducing system efficiently catalyzed a sequential three-component coupling of aliphatic carboxylic acids, aromatic carboxylic acids, and t-butyl mercaptan (t-butylthiol), to produce unsymmetrical dialkyl sulfides. With this reducing system, t-butyl mercaptan became a new source of sulfidation via an alkyl t-butyl sulfide that functioned as the reaction intermediate.
Selective reduction of thioacetal to sulfide by gallium(II) chloride
Ikeshita, Kei-Ichiro,Kihara, Nobuhiro,Ogawa, Akiya
, p. 8773 - 8775 (2007/10/03)
The reaction of dithioacetals with gallium(II) chloride followed by the acid treatment afforded sulfides in good yields.
