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- W2035595103 abstract "An oxygen–chlorine interaction is reported in the transition state of the Michael addition of acetone to nitrostyrene catalyzed by enantioenriched monosulfonamides. The interaction between the oxygen from the nitro group and the chlorine at the ortho-position of the sulfonamide moiety is supported by theoretical calculations. Asymmetric Michael addition products catalyzed by monosulfonamides were obtained in moderate yields and enantioselectivities." @default.
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- W2035595103 date "2014-07-01" @default.
- W2035595103 modified "2023-10-05" @default.
- W2035595103 title "Oxygen–chlorine interactions in the transition state of asymmetric Michael additions of carbonyl compounds to β-nitrostyrene" @default.
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- W2035595103 doi "https://doi.org/10.1016/j.tetasy.2014.05.002" @default.
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