Literature DB >> 25351145

Intramolecular redox reaction for the synthesis of N-aryl pyrroles catalyzed by Lewis acids.

Hong-Jin Du1, Le Zhen, Xiaoan Wen, Qing-Long Xu, Hongbin Sun.   

Abstract

An efficient approach to synthesize N-aryl pyrroles via Lewis acid-mediated 1,5-hydride shift and isomerization of 2-(3-pyrroline-1-yl)arylaldehydes has been achieved in up to 89% yield. This methodology is applicable to the synthesis of fluorazene derivatives as electron donor (D)/acceptor (A) molecules.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 25351145     DOI: 10.1039/c4ob02009j

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


  1 in total

1.  Lewis acid-catalyzed redox-neutral amination of 2-(3-pyrroline-1-yl)benzaldehydes via intramolecular [1,5]-hydride shift/isomerization reaction.

Authors:  Chun-Huan Jiang; Xiantao Lei; Le Zhen; Hong-Jin Du; Xiaoan Wen; Qing-Long Xu; Hongbin Sun
Journal:  Beilstein J Org Chem       Date:  2014-12-05       Impact factor: 2.883

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.