4.8 Article

Direct electrophilic monofluoromethylation

Journal

ORGANIC LETTERS
Volume 10, Issue 4, Pages 557-560

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol702500u

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Monofluoromethyl derivatives of various nucleophiles have been synthesized using a new electrophilic monofluoromethylating reagent developed. The S-(monofluoromethyl)diarylsulfonium tetrafluoroborate has been shown to be effective for the introduction of an electrophilic monofluoromethyl group into C, S, O, N, and P nucleophiles. This methodology has been expanded for the synthesis of various biologically important compounds.

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