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- W4246342009 abstract "Chlorine radical, which is classically generated by the homolysis of Cl2 under UV irradiation, can abstract a hydrogen atom from an unactivated C(sp3)−H bond. We herein demonstrate the use of HCl as an effective hydrogen-atom-transfer catalyst precursor activated by an organic acridinium photoredox catalyst under visible-light irradiation for C−H alkylation and allylation. The key to success relied on the utilization of microtubing reactors to maintain the volatile HCl catalyst. This photomediated chlorine-based C−H activation protocol is effective for a variety of unactivated C(sp3)−H bond patterns, even with primary C(sp3)−H bonds, as in ethane. The merit of this strategy is illustrated by rapid access to several pharmaceutical drugs from abundant unfunctionalized alkane feedstocks." @default.
- W4246342009 created "2022-05-12" @default.
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- W4246342009 date "2018-08-31" @default.
- W4246342009 modified "2023-10-01" @default.
- W4246342009 title "Microtubing-Reactor-Assisted Aliphatic C−H Functionalization with HCl as a Hydrogen-Atom-Transfer Catalyst Precursor in Conjunction with an Organic Photoredox Catalyst" @default.
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- W4246342009 doi "https://doi.org/10.1002/ange.201804844" @default.
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