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• W2214543896 startingPage "2304" @default.
• W2214543896 abstract "Tetrahydroquinolines () with an all-carbon quaternary stereocenter were effectively obtained via the in situ formation of aza-ortho-xylylene () with easily accessible 1,2-dihydroquinolines as precursors. The reaction was rationalized with chiral phosporic acid to afford chiral with high yield and excellent enantioselectivity." @default.
• W2214543896 created "2016-06-24" @default.
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• W2214543896 date "2016-01-01" @default.
• W2214543896 modified "2023-09-30" @default.
• W2214543896 title "The catalytic enantioselective synthesis of tetrahydroquinolines containing all-carbon quaternary stereocenters via the formation of aza-ortho-xylylene with 1,2-dihydroquinoline as a precursor" @default.
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• W2214543896 doi "https://doi.org/10.1039/c5cc07752d" @default.
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