2023Unpublished venueOpen access

A Versatile, Electrophilic Reagent for Monofluoromethylthiola-tion

Rui Wang, Long Lv, Qilong Shen

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Abstract

A new electrophilic monofluoromethylthiolating reagent N-fluoromethylthiophthalimide PhthSCH2F 1 was developed. Reagent 1 could be readily synthesized from easily available starting materials benzyl mercaptan and CH2FCl in three steps. N-fluoromethylthiophthalimide 1 is a powerful electrophilic monofluoromethylthiolating reagent that allows the monofluorome-thylthiolation of a wide range of nucleophiles including alkynes, aryl/vinyl boronic acids, electron-rich heteroarenes,-ketoesters and oxindoles, as well as thiols under mild conditions.

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A new electrophilic monofluoromethylthiolating reagent N-fluoromethylthiophthalimide PhthSCH2F 1 was developed. Reagent 1 could be readily synthesized from easily available starting materials benzyl mercaptan and CH2FCl in three steps. N-fluoromethylthiophthalimide 1 is a powerful electrophilic monofluoromethylthiolating reagent that allows the monofluorome-thylthiolation of a wide range of nucleophiles including alkynes, aryl/vinyl boronic acids, electron-rich heteroarenes,-ketoesters and oxindoles, as well as thiols under mild conditions.

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Available abstract

A new electrophilic monofluoromethylthiolating reagent N-fluoromethylthiophthalimide PhthSCH2F 1 was developed. Reagent 1 could be readily synthesized from easily available starting materials benzyl mercaptan and CH2FCl in three steps. N-fluoromethylthiophthalimide 1 is a powerful electrophilic monofluoromethylthiolating reagent that allows the monofluorome-thylthiolation of a wide range of nucleophiles including alkynes, aryl/vinyl boronic acids, electron-rich heteroarenes,-ketoesters and oxindoles, as well as thiols under mild conditions.

Key concepts: Reagent, Electrophile, Nucleophile, Aryl, Chemistry, Combinatorial chemistry, Organic chemistry, Catalysis

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