Literature DB >> 22968931

Biomimetic oxidative coupling of benzylamines and 2-aminophenols: synthesis of benzoxazoles.

Yoshinori Endo1, Jan-E Bäckvall.   

Abstract

Aerobic oxidation: in a biomimetic approach, a mixture of redox catalysts forms couples that effect the aerobic oxidation of a mixture of benzylamine and 2-aminophenol derivatives to give the corresponding benzoxazoles. This biomimetic oxidation proceeds smoothly under mild conditions and the protocol can also be used for preparing benzimidazoles and benzothiazoles.
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2012        PMID: 22968931     DOI: 10.1002/chem.201202187

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  3 in total

1.  A bioinspired catalytic aerobic oxidative C-H functionalization of primary aliphatic amines: synthesis of 1,2-disubstituted benzimidazoles.

Authors:  Khac Minh Huy Nguyen; Martine Largeron
Journal:  Chemistry       Date:  2015-07-23       Impact factor: 5.236

2.  Redox-Active Guanidines in Proton-Coupled Electron-Transfer Reactions: Real Alternatives to Benzoquinones?

Authors:  Ute Wild; Olaf Hübner; Hans-Jörg Himmel
Journal:  Chemistry       Date:  2019-09-19       Impact factor: 5.236

3.  Palladium-catalyzed oxidative regio- and diastereoselective diarylating carbocyclization of dienynes.

Authors:  Min Jiang; Jan-E Bäckvall
Journal:  Chemistry       Date:  2013-04-09       Impact factor: 5.236

  3 in total

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