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• W2060430627 endingPage "1662" @default.
• W2060430627 startingPage "1657" @default.
• W2060430627 abstract "In the presence of an (R)-MOP-Pd2(dba)3 catalyst, the reaction of ortho-tert-butylaniline with 2-bromophenyl arylethynyl ketone proceeded via a tandem amination (1,4-addition of aniline to an ynone and subsequent intramolecular Buchwald–Hartwig amination) to afford axially chiral N-(2-tert-butylphenyl)-2-aryl-4-quinolinone derivatives with moderate enantioselectivity (up to 72% ee)." @default.
• W2060430627 created "2016-06-24" @default.
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• W2060430627 date "2012-12-01" @default.
• W2060430627 modified "2023-10-18" @default.
• W2060430627 title "Catalytic enantioselective synthesis of atropisomeric 2-aryl-4-quinolinone derivatives with an N–C chiral axis" @default.
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• W2060430627 doi "https://doi.org/10.1016/j.tetasy.2012.11.004" @default.
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