Abstract
An unprecedented but challenging defluorinative arylboration has been achieved. Enabled by a copper catalyst, an interesting procedure on defluorinative arylboration of styrenes has been established. With polyfluoroarenes as the substrates, this methodology offers flexible and facile access to provide a diverse assortment of products under mild reaction conditions. In addition, by using a chiral phosphine ligand, an enantioselective defluorinative arylboration was also realized, affording a set of chiral products with unprecedented levels of enantioselectivity.
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CITATION STYLE
Wu, F. P., Gu, X. W., Geng, H. Q., & Wu, X. F. (2023). Copper-catalyzed defluorinative arylboration of vinylarenes with polyfluoroarenes. Chemical Science, 14(9), 2342–2347. https://doi.org/10.1039/d2sc06472c
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