Journal of Organic Chemistry p. 4623 - 4626 (1986)
Update date:2022-07-30
Topics: Stability Experimental
Weis, A. L.
Frolow, F.
Vishkautsan, R.
A series of 1,2- and 2,5-dihydropyrimidines was synthesized by LiAlH4 reduction of the corresponding pyrimidines.It was demonstrated that these compounds undergo imine-enamine tautomerism.The ratio as well as the stability of imine (2,5) or enamine (1,2)
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