@article{8c7d8089fbb74321913f025b49297f60,
title = "Thiyl-Radical-Catalyzed photoreductive hydrodifluoroacetamidation of alkenes with hantzsch ester as a multifunctional reagent",
abstract = "Hydrodifluoroacetamidation of alkenes with readily available α-bromodifluoroacetamides was achieved by means of a photoreductive reaction catalyzed by the phenyl thiyl radical. A Hantzsch ester was used as the hydrogen donor and electron donor. This photoreductive pathway did not involve the oxidation of a carbon radical intermediate to a carbocation species.",
keywords = "Difluoroacetamidation, Hnatzsch ester, Photoreductive, Thiyl radical, Visible light",
author = "Wenhao Huang and Wenxin Chen and Guoqiang Wang and Jin Li and Xu Cheng and Guigen Li",
note = "Funding Information: We are grateful for grants from the National Science Foundation of China (Nos. 21572099, 21332005), the Natural Science Foundation of Jiangsu Province (No. BK20151379). Publisher Copyright: {\textcopyright} 2016 American Chemical Society.",
year = "2016",
month = nov,
day = "4",
doi = "10.1021/acscatal.6b02420",
language = "English",
volume = "6",
pages = "7471--7474",
journal = "ACS Catalysis",
issn = "2155-5435",
publisher = "American Chemical Society (ACS)",
number = "11",
}