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- W2949470462 abstract "A quinine-derived thiourea organocatalyst promoted the highly enantioselective addition of naphthols and activated phenols to ketimines derived from isatins. The reaction afforded chiral 3-amino-2-oxindoles with a quaternary stereocenter in high yields (up to 99 %) with excellent enantioselectivity (up to 99 % ee). To the best of our knowledge, this transformation is the first highly enantioselective addition of naphthols to ketimines." @default.
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- W2949470462 date "2015-09-01" @default.
- W2949470462 modified "2023-10-15" @default.
- W2949470462 title "ChemInform Abstract: Organocatalytic Asymmetric Addition of Naphthols and Electron-Rich Phenols to Isatin-Derived Ketimines: Highly Enantioselective Construction of Tetrasubstituted Stereocenters." @default.
- W2949470462 cites W2153980917 @default.
- W2949470462 doi "https://doi.org/10.1002/chin.201538132" @default.
- W2949470462 hasPublicationYear "2015" @default.
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