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- W2905455220 abstract "A general and highly enantioselective Michael addition of malonates to cinnamones and chalcones has been developed. The commercially available 1,2-diphenylethanediamine could be directly utilized as the organocatalyst to furnish the desired adducts in satisfactory yield (61-99%) and moderate to excellent enantiopurity (65 to >99% ee). β-Ketoester was also a competent donor and was employed to construct densely functionalized cyclohexenones via a tandem Michael-aldol condensation process." @default.
- W2905455220 created "2018-12-22" @default.
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- W2905455220 date "2018-01-01" @default.
- W2905455220 modified "2023-09-26" @default.
- W2905455220 title "Enantioselective Michael addition of malonates to α,β-unsaturated ketones catalyzed by 1,2-diphenylethanediamine" @default.
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- W2905455220 doi "https://doi.org/10.1039/c8ra07809b" @default.
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