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Published in 2018 at "Organic letters"
DOI: 10.1021/acs.orglett.8b01760
Abstract: Direct visible-light-mediated aminofluorination of styrenes has been developed with high regioselectivity. Shelf-stable N-Ts-protected 1-aminopyridine salt was used as the nitrogen-radical precursor, and the commercially available hydrogen fluoride-pyridine was used as the nucleophilic fluoride source. The…
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Keywords:
olefins via;
component aminofluorination;
three component;
aminofluorination ... See more keywords