Electrophilic Trifluoromethylselenolation of Boronic Acids
AbstractTrifluoromethylselenylated compounds are emergent compounds with interesting physicochemical properties that still suffer from a lack of efficient synthetic methods. We recently developed an efficient one-pot strategy to generate in situ CF3SeCl and use it in various reactions. Herein, we continue our study of the reactivity scope of this preformed reagent. Cross-coupling reactions with aromatic and heteroaromatic boronic acids have been investigated. The expected products have been obtained, using a stoichiometric amount of copper, with moderate yields. View Full-Text
Scifeed alert for new publicationsNever miss any articles matching your research from any publisher
- Get alerts for new papers matching your research
- Find out the new papers from selected authors
- Updated daily for 49'000+ journals and 6000+ publishers
- Define your Scifeed now
Ghiazza, C.; Tlili, A.; Billard, T. Electrophilic Trifluoromethylselenolation of Boronic Acids. Molecules 2017, 22, 833.
Ghiazza C, Tlili A, Billard T. Electrophilic Trifluoromethylselenolation of Boronic Acids. Molecules. 2017; 22(5):833.Chicago/Turabian Style
Ghiazza, Clément; Tlili, Anis; Billard, Thierry. 2017. "Electrophilic Trifluoromethylselenolation of Boronic Acids." Molecules 22, no. 5: 833.
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.