Literature DB >> 29987306

N-Sulfonyl acetylketenimine as a highly reactive intermediate for the synthesis of N-sulfonyl amidines.

Weiguang Yang1, Dayun Huang, Xiaobao Zeng, Dongping Luo, Xinyan Wang, Yuefei Hu.   

Abstract

A highly reactive intermediate N-sulfonyl acetylketenimine was generated from a 3-butyn-2-one participating CuAAC/ring-opening method. Its high reactivity due to bearing two EWGs allowed us to offer the first example of a reaction between ketenimine and amide to synthesize N-sulfonyl amidines efficiently.

Entities:  

Year:  2018        PMID: 29987306     DOI: 10.1039/c8cc04699a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  5 in total

1.  Copper-catalyzed three-component reaction to synthesize polysubstituted imidazo[1,2-a]pyridines.

Authors:  Zitong Zhou; Danyang Luo; Guanrong Li; Zhongtao Yang; Liao Cui; Weiguang Yang
Journal:  RSC Adv       Date:  2022-07-14       Impact factor: 4.036

2.  Catalyst-free one-pot, four-component approach for the synthesis of di- and tri-substituted N-sulfonyl formamidines.

Authors:  Ai-Ran Liu; Lei Zhang; Jiao Li; Abudureheman Wusiman
Journal:  RSC Adv       Date:  2021-04-27       Impact factor: 3.361

3.  Preparation of 1,2-substituted benzimidazoles via a copper-catalyzed three component coupling reaction.

Authors:  Weiguang Yang; Yu Zhao; Zitong Zhou; Li Li; Liao Cui; Hui Luo
Journal:  RSC Adv       Date:  2021-02-25       Impact factor: 3.361

4.  Rapid and efficient synthesis of formamidines in a catalyst-free and solvent-free system.

Authors:  Zitong Zhou; Yu Zhao; Donghua Zhou; Li Li; Hui Luo; Liao Cui; Weiguang Yang
Journal:  RSC Adv       Date:  2021-10-18       Impact factor: 4.036

5.  A simple and efficient copper-catalyzed three-component reaction to synthesize (Z)-1,2-dihydro-2-iminoquinolines.

Authors:  Xiai Luo; Yu Zhao; Susu Tao; Zhong-Tao Yang; Hui Luo; Weiguang Yang
Journal:  RSC Adv       Date:  2021-09-29       Impact factor: 4.036

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.