A selected series of 2-(4-methylpyridin-2-yl)-1H-benzimidazole derivatives, bases and cyclic mono- and bis-salts, were synthesized. Complete H-1 nmr characterization is reported. Ambiguous assignments were solved using H-1-H-1 NOESY analysis. Significant ir and H-1 nmr data are presented concerning: i) tautomeric equilibrium of imidazole hydrogen; ii) hydrogen bonds; iii) conformational inversion of partially saturated rings.

2-(4-methylpyridin-2-yl)-1H-benzimidazole derivatives. Part II, H-1 nmr characterization

BARNI, Ermanno;BAROLO, CLAUDIA;QUAGLIOTTO, Pierluigi;SAVARINO, Piero;VISCARDI, Guido;MARABELLO, Domenica
2003-01-01

Abstract

A selected series of 2-(4-methylpyridin-2-yl)-1H-benzimidazole derivatives, bases and cyclic mono- and bis-salts, were synthesized. Complete H-1 nmr characterization is reported. Ambiguous assignments were solved using H-1-H-1 NOESY analysis. Significant ir and H-1 nmr data are presented concerning: i) tautomeric equilibrium of imidazole hydrogen; ii) hydrogen bonds; iii) conformational inversion of partially saturated rings.
2003
40
649
654
BIS-QUATERNARY SALTS; HETEROCYCLIC-SYSTEMS; METHYLPYRIDYLBENZIMIDAZOLES; 2-METHYLPYRIDYL; BENZOTHIAZOLES; COMPLEXES; BEHAVIOR; DYES; MONO
E. BARNI; C. BAROLO; P. QUAGLIOTTO; P. SAVARINO; G. VISCARDI; D. MARABELLO
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/38007
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