Issue 9, 2017

Three-component difunctionalization of alkenes leading to β-acetamido sulfides and β-acetoxy sulfides

Abstract

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.

Graphical abstract: Three-component difunctionalization of alkenes leading to β-acetamido sulfides and β-acetoxy sulfides

Supplementary files

Article information

Article type
Paper
Submitted
16 Jan 2017
Accepted
03 Feb 2017
First published
03 Feb 2017

Org. Biomol. Chem., 2017,15, 1998-2002

Three-component difunctionalization of alkenes leading to β-acetamido sulfides and β-acetoxy sulfides

D. Wang, Z. Yan, Q. Xie, R. Zhang, S. Lin and Y. Wang, Org. Biomol. Chem., 2017, 15, 1998 DOI: 10.1039/C7OB00110J

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