Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 16, Issue 44, Pages 8565-8568Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ob02431f
Keywords
-
Categories
Funding
- Shandong Provincial Natural Science Foundation of China [ZR2016BQ31, ZR2016HM44, ZR2016JL009]
- Shandong Key Research Program of China [2017GSF218061]
- Major Program of Shandong Province Natural Science Foundation of China [ZR2017ZC0529]
- University of Jinan
Ask authors/readers for more resources
Difluoromethylthiolation of aryldiazonium salts under photocatalytic conditions with a shelf-stable, easily prepared and inexpensive reagent, PhSO2SCF2H was described. A variety of difluoromethylthioethers were obtained utilizing aryldiazonium salts containing different functional groups. Aryldiazonium salts with a heteroarene moiety were tolerated. Fluorescence quenching experiments indicated that both oxidative and reductive quenching cycles occurred during this process.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available
Share Paper
