Photoredox catalyzed C–H trifluoroethylamination of heteroarenes†
Abstract
The first C–H trifluoroethylamination of heteroarenes with previously unknown N-trifluoroethyl hydroxylamine reagents was achieved under photoredox catalyzed conditions. In the presence of an iridium(III) photoredox catalyst, a variety of heteroarenes, such as indoles, benzofurans, and benzothiophenes, were smoothly converted to the trifluoroethylaminated products in moderate to high yields and with excellent regioselectivity.
- This article is part of the themed collection: 10th Anniversary of the Youth Innovation Promotion Association of the Chinese Academy of Science