Literature DB >> 24519720

Synthesis of highly functionalized diaryl ethers by copper-mediated O-arylation of phenols using trivalent arylbismuth reagents.

Cynthia Crifar1, Pauline Petiot, Tabinda Ahmad, Alexandre Gagnon.   

Abstract

Highly functionalized diaryl ethers were prepared by copper(II) acetate mediated O-arylation reaction of phenols using trivalent organobismuthanes. The reaction is performed under simple conditions and tolerates a wide diversity of functional groups on the phenol and on the organobismuth reagent. Substoichiometric amounts of catalyst can be used by performing the reaction under an oxygen atmosphere. The N-arylation of pyridones is also reported.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  O-arylation; copper catalysis; functionalized diaryl ethers; phenols; triarylbismuthanes

Mesh:

Substances:

Year:  2014        PMID: 24519720     DOI: 10.1002/chem.201303684

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


  2 in total

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Authors:  Mark Jurrat; Lorenzo Maggi; William Lewis; Liam T Ball
Journal:  Nat Chem       Date:  2020-02-27       Impact factor: 24.427

2.  Crystal structure of pirfenidone (5-methyl-1-phenyl-1H-pyridin-2-one): an active pharmaceutical ingredient (API).

Authors:  Mauro Barbero; Matteo Mossotti; Angelo Sironi; Giovanni Battista Giovenzana; Valentina Colombo
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2019-06-11
  2 in total

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