| Literature DB >> 24519720 |
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.Entities:
Keywords: O-arylation; copper catalysis; functionalized diaryl ethers; phenols; triarylbismuthanes
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Year: 2014 PMID: 24519720 DOI: 10.1002/chem.201303684
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236