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- W4205501932 abstract "This study investigates the photo-induced C–X borylation reaction of aryl halides by forming a halogen-bonding complex. The method employs 2-naphthol as a halogen-bonding acceptor and proceeds under mild conditions without a photoredox catalyst under 420 nm blue light irradiation. The method is highly chemoselective, broadly functional group tolerant, and provides concise access to corresponding boronate esters. Mechanistic studies reveal that forming the halogen-bonding complex between aryl halide and naphthol acts as an electron donor-acceptor complex to furnish aryl radicals through photo-induced electron transfer." @default.
- W4205501932 created "2022-01-26" @default.
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- W4205501932 date "2022-01-06" @default.
- W4205501932 modified "2023-09-26" @default.
- W4205501932 title "Halogen-bonding-promoted Photo-induced C–X Borylation of Aryl Halide using Phenol Derivatives" @default.
- W4205501932 doi "https://doi.org/10.26434/chemrxiv-2022-glvkg" @default.
- W4205501932 hasPublicationYear "2022" @default.
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