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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b01428
Abstract: A practical synthesis of α-fluorinated imides via the catalyst-free fluorohydroxylation of ynamides is developed. The reaction employs commercially available Selectfluor (F-TEDA-BF4) and H2O as the fluorine and hydroxyl sources, respectively. A broad range of aryl-…
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Keywords:
synthesis fluorinated;
fluorohydroxylation ynamides;
via direct;
fluorinated imides ... See more keywords