1455451-38-3Relevant academic research and scientific papers
Three-component difunctionalization of alkenes leading to β-acetamido sulfides and β-acetoxy sulfides
Wang, Dingyi,Yan, Zhaohua,Xie, Qihuang,Zhang, Rongxing,Lin, Sen,Wang, Yuanxing
, p. 1998 - 2002 (2017)
A novel method for the synthesis of β-acetamido sulfides via NBS-mediated aminosulfenylation of alkenes with thiophenols and nitriles under metal-free conditions has been described. And β-acetamido sulfides were also synthesized with 1-(arylthio)pyrrolidine-2,5-diones as substrates and HBr as an additive. On the other hand, iodine-catalyzed 1,2-acetoxysulfenylation of alkenes by using (diacetoxyiodo)benzene as an oxygen source to synthesise various β-acetoxy sulfides was described as well.
PhI(OAc)2/KI mediated 1,2-acetoxysulfenylation of alkenes: Facile synthesis of β-acetoxysulfides
Muangkaew, Charoensak,Katrun, Praewpan,Kanchanarugee, Patcharaphon,Pohmakotr, Manat,Reutrakul, Vichai,Soorukram, Darunee,Jaipetch, Thaworn,Kuhakarn, Chutima
, p. 8847 - 8856 (2013/09/23)
A convenient method for 1,2-acetoxysulfenylation of alkenes using disulfide promoted by (diacetoxyiodo)benzene (PhI(OAc)2, DIB)/KI was developed. The reaction is highly regioselective for styrene derivatives while aliphatic alkenes lead to a mixture of two regioisomers.
