95062-79-6Relevant articles and documents
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.
Single-step thioetherification by indium-catalyzed reductive coupling of carboxylic acids with thiols
Sakai, Norio,Miyazaki, Takahiro,Sakamoto, Tomohiro,Yatsuda, Takuma,Moriya, Toshimitsu,Ikeda, Reiko,Konakahara, Takeo
, p. 4366 - 4369 (2012/10/29)
Direct thioetherification from a variety of aromatic carboxylic acids and thiols using a reducing system combined with InBr3 and 1,1,3,3-teramethyldisiloxane (TMDS) in a one-pot procedure is demonstrated. It was also found that a system combine
