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- W2952384013 abstract "The organocatalytic asymmetric Michael addition of aldehydes to a nitro olefin in aqueous organic solvents catalysed by a broad range of simple primary amines and amino alcohols is reported. In particular, the use of (S,S)-diphenylethylenediamine, which is the chiral backbone of various organocatalysts, gave addition products in good yields and with good to high enantioselectivities (45–96 % ee). Remarkably high enantioselectivities were observed for the demanding conjugate addition of α,α-disubstituted aldehydes to nitrostyrene (96–98 % ee) in aqueous organic solvent mixtures." @default.
- W2952384013 created "2019-06-27" @default.
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- W2952384013 date "2016-01-02" @default.
- W2952384013 modified "2023-10-18" @default.
- W2952384013 title "ChemInform Abstract: Unmodified Primary Amine Organocatalysts for Asymmetric Michael Reactions in Aqueous Media." @default.
- W2952384013 cites W1577924037 @default.
- W2952384013 doi "https://doi.org/10.1002/chin.201602029" @default.
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