| Literature DB >> 27860031 |
Tohru Kamitanaka1, Koji Morimoto2, Kohei Tsuboshima2, Daichi Koseki2, Hitoho Takamuro2, Toshifumi Dohi2, Yasuyuki Kita1.
Abstract
A simple and efficient synthesis of phenol biaryls by the cross-couplings of quinone monoacetals (QMAs) and phenols is reported. The Brønsted acid catalytic system in 1,1,1,3,3,3-hexafluoro-2-propanol was found to be particularly efficient for this transformation. This reaction can be extended to the synthesis of various phenol biaryls, including sterically hindered biaryls, with yields ranging from 58 to 90 % under mild reaction conditions and in a highly regiospecific manner.Entities:
Keywords: Brønsted acid; biaryls; cross-coupling; phenols; reaction mechanisms
Year: 2016 PMID: 27860031 DOI: 10.1002/anie.201608013
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336