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Published in 2017 at "Synlett"
DOI: 10.1055/s-0036-1589057
Abstract: We report that aromatic propargylation is achievable with secondary propargylic fluorides, thus affording 1-alkyl-1-aryl-2-alkynes. In the present case, hydrogen bonding is responsible for the activation of the C–F bond. A large excess of arene nucleophile…
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Keywords:
secondary propargylic;
hydrogen bond;
aryl alkynes;
propargylic fluorides ... See more keywords