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- W2045771012 abstract "Abstract Michael addition of the dienolate derived from 2-butenoic acid to 1,3-diphenylpro-penone occurs through a 1,2-addition followed by a 3 ,3-sigmatropic rearrangement. α,γ -re-gioselectivity found for Michael addition to other styryl ketones depends on the steric parameter of the substituents at the carbonyl group, in agreement with the same tandem addition rearrangement mechanism." @default.
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- W2045771012 date "1985-01-01" @default.
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- W2045771012 title "Unsaturated carboxylic acid dienolates. Michael addition to enones through tandem 1,2-addition - oxy-cope rearrangement." @default.
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- W2045771012 doi "https://doi.org/10.1016/s0040-4039(00)94860-3" @default.
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