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The first successful example of the stereoselective conjugate addition of azlactones to ynones is reported. Diaminomethylenemalononitrile organocatalysts efficiently promoted the asymmetric conjugate addition of azlactones to ynones, affording the corresponding α-vinyl quaternary α-amino acid derivatives in high yields with good to high enantioselectivities (up to 91% ee).
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Iino et al. (2026) studied this question.
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