Catalytic enantioselective fluorination reactions of α-cyano acetates and α-cyanophosphonates using chiral palladium complexes

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Abstract

The catalytic enantioselective electrophilic fluorinations of active methane compounds promoted chiral palladium complexes have been developed. Treatment of α-cyano acetates and α-cyanoalkylphosphonates with N-fluorobenzenesulfonimide as the fluorine source under mild reaction conditions afforded the corresponding α-cyano-α-fluorinated adducts in high yields with excellent enantiomeric excesses (up to 99% ee). These reactions can be conducted in alcoholic solvents without any precaution to exclude water and moisture.

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Kim, S. M., Kang, Y. K., Cho, M. J., Mang, J. Y., & Kim, D. Y. (2007). Catalytic enantioselective fluorination reactions of α-cyano acetates and α-cyanophosphonates using chiral palladium complexes. Bulletin of the Korean Chemical Society, 28(12), 2435–2441. https://doi.org/10.5012/bkcs.2007.28.12.2435

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