| Literature DB >> 27959520 |
Tolani K Salvador1,2, Charles H Arnett1, Subrata Kundu1, Nicholas G Sapiezynski1, Jeffery A Bertke1, Mahdi Raghibi Boroujeni1, Timothy H Warren1.
Abstract
A variety of acyl protected phenols AcOAr participate in sp3 C-H etherification of substrates R-H to give alkyl aryl ethers R-OAr employing tBuOOtBu as oxidant with copper(I) β-diketiminato catalysts [CuI]. Although 1°, 2°, and 3° C-H bonds may be functionalized, selectivity studies reveal a preference for the construction of hindered, 3° C-OAr bonds. Mechanistic studies indicate that β-diketiminato copper(II) phenolates [CuII]-OAr play a key role in this C-O bond forming reaction, formed via transesterification of AcOAr with [CuII]-OtBu intermediates generated upon reaction of [CuI] with tBuOOtBu.Entities:
Year: 2016 PMID: 27959520 DOI: 10.1021/jacs.6b09057
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419