Tautomeric Equilibria in Solutions of 2-Phenacylbenzimidazoles
Detailed NMR spectral analysis of DMSO-d6 solutions of the series of substituted 2-phenacylbenzimidazoles (ketimine form, K) reveals two from three tautomeric forms. Integrals of the 1H NMR signals are used in establishing the molar ratio of tautomers. The experimental analyses are supported by quan...
Main Authors: | Agnieszka Skotnicka, Przemysław Czeleń, Ryszard Gawinecki |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2019-01-01
|
Series: | Heteroatom Chemistry |
Online Access: | http://dx.doi.org/10.1155/2019/4364207 |
Similar Items
-
Substituted 2-Phenacylbenzoxazole Difluoroboranes: Synthesis, Structure and Properties
by: Agnieszka Skotnicka, et al.
Published: (2020-11-01) -
Using Chou’s 5-Step Rule to Evaluate the Stability of Tautomers: Susceptibility of 2-[(Phenylimino)-methyl]-cyclohexane-1,3-diones to Tautomerization Based on the Calculated Gibbs Free Energies
by: Robert Dobosz, et al.
Published: (2020-01-01) -
Quantum-chemical modeling of the tautomeric equilibria of modified anionic nucleic acid bases
by: Mati Karelson, et al.
Published: (2002-04-01) -
ADMET and Solubility Analysis of New 5-Nitroisatine-Based Inhibitors of CDK2 Enzymes
by: Przemysław Czeleń, et al.
Published: (2023-11-01) -
2-Methyl-4-phenyl-3,4-dihydroquinazoline
by: Arto Valkonen, et al.
Published: (2011-04-01)