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• W2610946989 abstract "The intermolecular alkylation of pyridine units with simple alkenes has been achieved via a photoredox radical mechanism. This process occurs with complete regiocontrol, where single-electron reduction of halogenated pyridines regiospecifically yields the corresponding radicals in a programmed fashion, and radical addition to alkene substrates occurs with exclusive anti-Markovnikov selectivity. This system is mild, tolerant of many functional groups, and effective for the preparation of a wide range of complex alkylpyridines." @default.
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• W2610946989 date "2017-05-09" @default.
• W2610946989 modified "2023-10-17" @default.
• W2610946989 title "Anti-Markovnikov Hydroarylation of Unactivated Olefins via Pyridyl Radical Intermediates" @default.
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• W2610946989 doi "https://doi.org/10.1021/jacs.7b03262" @default.
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