Literature DB >> 28181596

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

Dingyi Wang1, Zhaohua Yan1, Qihuang Xie1, Rongxing Zhang1, Sen Lin1, Yuanxing Wang2.   

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.

Entities:  

Year:  2017        PMID: 28181596     DOI: 10.1039/c7ob00110j

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Electrochemical oxidative oxysulfenylation and aminosulfenylation of alkenes with hydrogen evolution.

Authors:  Yong Yuan; Yixuan Chen; Shan Tang; Zhiliang Huang; Aiwen Lei
Journal:  Sci Adv       Date:  2018-08-03       Impact factor: 14.136

  1 in total

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