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

✍ Scribed by Ermanno Barni; Claudia Barolo; Pierluigi Quagliotto; Piero Savarino; Guido Viscardi; Domenica Marabello


Book ID
102340955
Publisher
Journal of Heterocyclic Chemistry
Year
2003
Tongue
English
Weight
66 KB
Volume
40
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

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


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2-(4-methylpyridin-2-yl)-1H-benzimidazol
✍ Giuliana Gervasio; Domenica Marabello; Claudia Barolo; Pierluigi Quagliotto; Gui 📂 Article 📅 2003 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 58 KB

## Abstract The X‐ray analyses of some neutral and cationic derivatives of 2‐(4‐methylpyridin‐2‐yl)‐1__H__‐benzimida‐zole are reported and the structural data tentatively correlated to relative UV‐visible properties. A rotation of the γ‐picoline ring with respect to the benzimidazole moiety may be