Palladium-catalyzed Sonogashira coupling to synthesis of gem‑difluoroenynes

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Abstract

Herein, we developed the palladium-catalyzed Sonogashira-type cross-coupling of 1‑bromo-2,2-difluoroethylene with a variety of aromatic and aliphatic terminal alkynes proceeds smoothly at mild reaction condition to access the corresponding gem‑difluoroenyne derivatives. 1-Bromo-2,2-difluoroethylene is a useful difluoroethenyl source because of its commercially available and easy-to-handle. This new synthetic protocol provided a novel strategy to directly construct gem‑difluoroenynes with good functional group tolerance and high yields.

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Li, L., Mei, Y., Zhang, J., He, K., & Pan, F. (2023). Palladium-catalyzed Sonogashira coupling to synthesis of gem‑difluoroenynes. Journal of Fluorine Chemistry, 268. https://doi.org/10.1016/j.jfluchem.2023.110111

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