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- W2950253704 abstract "Three novel C-2-symmetrical chiral primary amines were synthesized from chiral BINOL and diamines. Then their catalytic activities in the asymmetric aldol reactions were evaluated, and the result indicated that 1c was the optimal organocatalyst. The reaction of a variety of aromatic aldehydes with aliphatic ketones, catalyzed by 20 mol % 1c in the addition of benzoic acid in carbon tetrachloride, afforded the aldol products in high yields (up to 92%) and good enantioselectivities (up to 71%)." @default.
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- W2950253704 date "2010-01-01" @default.
- W2950253704 modified "2023-09-27" @default.
- W2950253704 title "Direct Asymmetric Aldol Reaction Catalyzed by C2-Symmetrical Chiral Primary Amine Organocatalysts" @default.
- W2950253704 doi "https://doi.org/10.2174/157017810790533904" @default.
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