Your browser doesn't support javascript.
loading
Electrochemical Synthesis of 2-Aryl-3-(2-aminoaryl)quinoxalines via Oxidative Dearomatization/Ring-Opening/Cyclization Cascade Sequence of 2-Arylindoles with 1,2-Diaminoarenes.
Nagare, Yadav Kacharu; Yadav, Jyothi; Dolas, Atul Jankiram; Shah, Imtiyaz Ahmad; Rangan, Krishnan; Choudhary, Rahul; Iype, Eldhose; Kumar, Indresh.
Afiliação
  • Nagare YK; Department of Chemistry, Birla Institute of Technology and Science, Pilani 333031, Rajasthan, India.
  • Yadav J; Department of Chemistry, Birla Institute of Technology and Science, Pilani 333031, Rajasthan, India.
  • Dolas AJ; Department of Chemistry, Birla Institute of Technology and Science, Pilani 333031, Rajasthan, India.
  • Shah IA; Department of Chemistry, Birla Institute of Technology and Science, Pilani 333031, Rajasthan, India.
  • Rangan K; Department of Chemistry, Birla Institute of Technology and Science, Hyderabad 500078, Telangana, India.
  • Choudhary R; Praveen Laboratories Pvt. Ltd., Surat 394304, Gujrat, India.
  • Iype E; College of Engineering and Technology, American University of the Middle East, Egaila 54200, Kuwait.
  • Kumar I; Department of Chemistry, Birla Institute of Technology and Science, Pilani 333031, Rajasthan, India.
J Org Chem ; 88(15): 11111-11121, 2023 Aug 04.
Article em En | MEDLINE | ID: mdl-37489614
ABSTRACT
A straightforward method has been developed to synthesize 2-aryl-3-(2-aminoaryl) quinoxalines from 2-arylindoles and 1,2-diaminoarenes under mild electrochemical conditions. The reaction proceeds through in situ generations of 2-arylindole-3-ones under electrochemical oxidative dearomatization of 2-arylindoles, followed by a ring opening-cyclization sequence with 1,2-diaminoarenes. A series of 2-aryl-3-(2-aminoaryl) quinoxalines have been prepared with moderate to good yields (up to 75%).

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article