
Trifluoromethylselenylated 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.
boronic acids, Molecular Structure, Organic chemistry, trifluoromethylselenolation; boronic acids; trifluoromethylselenyl chloride; fluorine; selenium, Fluorine, Boronic Acids, Article, Catalysis, trifluoromethylselenyl chloride, QD241-441, fluorine, Organoselenium Compounds, [CHIM] Chemical Sciences, trifluoromethylselenolation, selenium, Copper
boronic acids, Molecular Structure, Organic chemistry, trifluoromethylselenolation; boronic acids; trifluoromethylselenyl chloride; fluorine; selenium, Fluorine, Boronic Acids, Article, Catalysis, trifluoromethylselenyl chloride, QD241-441, fluorine, Organoselenium Compounds, [CHIM] Chemical Sciences, trifluoromethylselenolation, selenium, Copper
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