Issue 0, 1984

Dihydroimidazoles in synthesis: C-acylation of lithiodihydroimidazoles

Abstract

1-Benzyl-2-methyl-4,5-dihydrpimidazole has been lithiated and C-acylated by reaction with esters and a nitrile. The products do not exist as 2-(2-oxoalkyl)dihydroimidazoles but as the alternative tautomers, as indicated by spectroscopic and crystallographic data.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1984, 2599-2602

Dihydroimidazoles in synthesis: C-acylation of lithiodihydroimidazoles

M. W. Anderson, M. J. Begley, R. C. F. Jones and J. Saunders, J. Chem. Soc., Perkin Trans. 1, 1984, 2599 DOI: 10.1039/P19840002599

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