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Axially Chiral C2-Symmetric N-Heterocyclic Carbene (NHC) Palladium Complex-Catalyzed Asymmetric Fluorination and Amination of Oxindoles

Axially Chiral C2-Symmetric N-Heterocyclic Carbene (NHC) Palladium Complex-Catalyzed Asymmetric Fluorination and Amination of Oxindoles
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摘要 Chiral C2-symmetric N-heterocyclic carbene (NHC) palladium diaquo complex 5b prepared from (S)-BINAM was found to be a fairly effective catalyst for the enantioselective asymmetric fluorination of oxindoles to give the corresponding products in moderate enantioselectivities along with good to excellent yields. Chiral C2-symmetric N-heterocyclic carbene (NHC) palladium diaquo complex 5b prepared from (S)-BINAM was found to be a fairly effective catalyst for the enantioselective asymmetric fluorination of oxindoles to give the corresponding products in moderate enantioselectivities along with good to excellent yields.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2012年第6期1295-1304,共10页 中国化学(英文版)
关键词 chiral C2-symmetric N-heterocyclic carbene (NHC) palladium diaquo complex (S)-B1NAM asym-metric fluorination of oxindoles N-fluorobenzenesulfonimide (NFSI) 1-chloromethyl-4-fluoro-l 4-diazoniabi-cyclo[2.2.2]octane bis(tetrafluoroborate) (selectfluor) chiral C2-symmetric N-heterocyclic carbene (NHC) palladium diaquo complex, (S)-B1NAM, asym-metric fluorination of oxindoles, N-fluorobenzenesulfonimide (NFSI), 1-chloromethyl-4-fluoro-l,4-diazoniabi-cyclo[2.2.2]octane bis(tetrafluoroborate) (selectfluor)
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