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• W2155368894 abstract "A robust binaphthyl-based amino acid ((S)-1) exhibits higher stability and selectivity than proline for the catalysis of a direct asymmetric aldol reaction between aldehydes and acetone (see scheme; DMF=N,N-dimethylformamide). Olefinic, heteroaromatic, and aromatic aldehydes were found to be suitable substrates, with the corresponding aldol adducts being obtained in good yields and excellent enantioselectivities." @default.
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• W2155368894 date "2005-05-09" @default.
• W2155368894 modified "2023-10-16" @default.
• W2155368894 title "Design of an Axially Chiral Amino Acid with a Binaphthyl Backbone as an Organocatalyst for a Direct Asymmetric Aldol Reaction" @default.
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• W2155368894 doi "https://doi.org/10.1002/anie.200500408" @default.
• W2155368894 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15828036" @default.
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