Literature DB >> 26863185

Synthesis of Quinoxaline Derivatives via Tandem Oxidative Azidation/Cyclization Reaction of N-Arylenamines.

Haichao Ma1, Dianjun Li1, Wei Yu1.   

Abstract

A new method was developed for the synthesis of quinoxalines. This method employs N-arylenamines and TMSN3 as the starting materials and implements two oxidative C-N bond-forming processes in a tandem pattern by using (diacetoxyiodo)benzene as the common oxidant. The present reaction conditions are mild and simple and thus are useful in practical synthesis.

Entities:  

Year:  2016        PMID: 26863185     DOI: 10.1021/acs.orglett.6b00148

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

1.  Facile, eco-friendly, catalyst-free synthesis of polyfunctionalized quinoxalines.

Authors:  Yaohong Zhang; Mengqiang Luo; Yan Li; Hai Wang; Xiaorong Ren; Chenze Qi
Journal:  Mol Divers       Date:  2017-10-05       Impact factor: 2.943

Review 2.  Metal-Catalysed Azidation of Organic Molecules.

Authors:  Monalisa Goswami; Bas de Bruin
Journal:  European J Org Chem       Date:  2016-12-22

Review 3.  Methods for direct C(sp2)-H bonds azidation.

Authors:  Ying Liu; Abdol Ghaffar Ebadi; Leila Youseftabar-Miri; Akbar Hassanpour; Esmail Vessally
Journal:  RSC Adv       Date:  2019-08-13       Impact factor: 4.036

4.  PIDA-mediated intramolecular oxidative C-N bond formation for the direct synthesis of quinoxalines from enaminones.

Authors:  Hong Zhang; Jinhai Shen; Zhenhui Yang; Xiuling Cui
Journal:  RSC Adv       Date:  2019-03-07       Impact factor: 4.036

  4 in total

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