Vinylamine—XX: Vergleich von imin-enamin-und keto-enol-tautomerie bei 2-aryl-2-methyl-vinylaminen und vinylalkoholen
H Ahlbrecht, W Funk, MT Reiner
Index: Ahlbrecht,H. et al. Tetrahedron, 1976 , vol. 32, p. 479 - 482
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Citation Number: 18
Abstract
Substituted 2-aryl-propionaldehydes tautomerize in dimethyl sulfoxide to the corresponding enoles. The ratio of the tautomers can be described by Hammett σ-values, as in the case of imin-enamine-tautomeric 2-aryl-propionaldehyde methylimines. This is the first example of a linear free energy relationship between the two forms of tautomerism.
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