Issue 6, 1970

Heterocyclic syntheses. Part XXIII. Synthesis and reactions of 2,3-dihydrobenzimidazoles

Abstract

1,2-Dialkyl-2,3-dihydrobenzimidazoles have been produced by reduction of the aromatic parent compounds with lithium aluminium hydride and also directly by cyclization of the appropriate nitrenes generated from azides or from nitro-compounds by deoxygenation with trialkyl phosphites. The factors influencing the stability of the title compounds have been studied.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 825-829

Heterocyclic syntheses. Part XXIII. Synthesis and reactions of 2,3-dihydrobenzimidazoles

R. Garner, G. V. Garner and H. Suschitzky, J. Chem. Soc. C, 1970, 825 DOI: 10.1039/J39700000825

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