Researches on pyrimidines. CXV. Alkylation on nitrogen of the pyrimidine cycle by application of a new technique involving molecular rearrangements

GE Hilbert, TB Johnson

Index: Hilbert; Johnson Journal of the American Chemical Society, 1930 , vol. 52, p. 2001,2006

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Citation Number: 105

Abstract

That the lactim ethers I will undergo rearrangements to their isomeric and stable Zactam configurations I1 has been known for a long time. These transformations are not reversible and are brought about by the application of heat or through the influence of special catalytic agents, and have been observed to take place in both the acyclic and cyclic series of organic compounds.*.