| Literature DB >> 26879796 |
Koji Morimoto1,2, Kazuma Sakamoto1, Takao Ohshika1, Toshifumi Dohi1, Yasuyuki Kita3,4.
Abstract
The direct oxidative coupling reaction has been an attractive tool for environmentally benign chemistry. Reported herein is that the hypervalent iodine catalyzed oxidative metal-free cross-coupling reaction of phenols can be achieved using Oxone as a terminal oxidant in 1,1,1,3,3,3-hexafluoropropan-2-ol (HFIP). This method features a high efficiency and regioselectivity, as well as functional-group tolerance under very mild reaction conditions without using metal catalysts.Entities:
Keywords: biaryls; cross-coupling; homogenous catalysis; iodine; oxidation
Year: 2016 PMID: 26879796 DOI: 10.1002/anie.201511007
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336