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• W1970562725 abstract "A highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinone to β-nitrostyrenes has been achieved using a novel class of sugar-Cinchona thiourea conjugates. The method offers significant advantages such as low catalyst loading (1 mol%), high enantioselectivity (up to 99% ee), short reaction times and ambient reaction conditions." @default.
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• W1970562725 date "2013-01-01" @default.
• W1970562725 modified "2023-10-09" @default.
• W1970562725 title "Sugar thiourea catalyzed highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinone to β-nitroalkenes" @default.
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• W1970562725 doi "https://doi.org/10.1039/c2ra22270a" @default.
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