Abstract
The asymmetric fluorination of β-keto esters with N-fluorobisbenzenesulphonimide (NFSI) catalyzed by a PEG-bound urea-containing chiral quaternary ammonium salt is developed. The corresponding products were obtained in good yields and enantioselectivities. The catalyst structure facilitated its recovery and multiple reuse without any loss of activity.
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Zhang, B., Shi, L., Guo, R., & Liu, S. (2016). Enantioselective fluorination of β-keto esters using a PEG-bound urea-containing chiral quaternary ammonium salt catalyst. Arkivoc, 2016(4), 363–370. https://doi.org/10.3998/ark.5550190.p009.420
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