Lewis Acid Promoted Vicinal Oxytrifluoromethylselenolation of Alkenes.
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DOI: 10.1021/acs.orglett.3c00846
Abstract: Herein, we have developed a metal-free, Lewis acid promoted vicinal oxytrifluoromethylselenolation of alkenes using trifluoromethyl selenoxides as electrophilic trifluoromethylselenolation reagents and alcohols as nucleophiles. With less steric and good nucleophilic solvents (such as ethanol and… read more here.
Keywords: oxytrifluoromethylselenolation alkenes; oxytrifluoromethylselenolation; acid promoted; promoted vicinal ... See more keywords