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- W2024342192 abstract "Abstract The regio- and diastereoselectivity of the addition of N,N-dialkylphenylthioacetamide enolates to some conjugate carbonyl compounds are studied. The results are compared with oxoanalogs and the differences are rationalized in terms of specific behaviour of sulfur. General trend to 1,4-addition is demonstrated. The stereochemistry is correlated with the cyclic transition state taking into account the ground state conformation preferred by the acceptor." @default.
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- W2024342192 date "1993-05-01" @default.
- W2024342192 modified "2023-09-24" @default.
- W2024342192 title "N,N-DIALKYLTHIOAMIDES IN THE MICHAEL ADDITION TO CONJUGATE CARBONYL COMPOUNDS, REGIOSELECTIVITY, STEREOCHEMISTRY AND MECHANISM" @default.
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- W2024342192 doi "https://doi.org/10.1080/10426509308032434" @default.
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