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https://doi.org/10.1002/cjoc.201100445
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Cite Journal: Chinese Journal of Chemistry |  Publication Date: Jan 1, 2012 |
 Citations: 11 |
Affiliation: Tianjin University
AbstractA facile and direct fluorination process of alkynes and diynes was developed. In the presence of n‐butyllithium, the reaction of a series of terminal alkynes and diynes with the electrophilic fluorinating reagent (NFSI) proceeded to afford various 1‐fluoroalkynes and 1‐fluoro‐1,3‐diynes in moderate to high yields.
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