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- W2024698123 abstract "Asymmetric conjugate addition to prochiral cycloalkenones was examined by utilizing a zinc azaenolate as well as a copper one derived from an acetone imine of optically active erythro-2-methoxy-1,2-diphenylethylamine, the best enantioselectivity of the resulting 3-acetonylcycloalkanones being as high as 92% ee." @default.
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- W2024698123 title "Asymmetric conjugate addition of zincates or cuprates containing an optically active azaenolate of erythro-isopropylidene-2-methoxy-1,2-diphenylamine to 2-cycloalkenones" @default.
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