Journal
TETRAHEDRON LETTERS
Volume 60, Issue 27, Pages 1796-1799Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2019.06.002
Keywords
Trifluoromethylselenolation; Ferric chloride-promoted; Indole; Se-(trifluoromethyl) 4-methylbenzenesulfonoselenoate
Categories
Funding
- National Natural Science Foundation of China [21572158]
- Tianjin Natural Science Foundation [18JCQNJC76600]
Ask authors/readers for more resources
The ferric chloride-promoted direct trifluoromethylselenolation of indoles and other nitrogen-containing heterocyclic compounds in water was performed by employing TsSeCF3 as a trifluoromethylselenolation reagent. The shelf-stable and readily accessible reagents, along with the environmentally friendly and mild reaction conditions make this method an effective alternative for the trifluoromethylselenolation of electron-rich aromatics. (C) 2019 Elsevier Ltd. All rights reserved.
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