1H-NMR study on the tautomer ratios between the hydrazone imine and diazenylenamine forms in 3-(arylhydrazono)-methyl-2-oxo-1,2-dihydroquinoxalines
Author:
Publisher
Wiley
Subject
Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.5570330234/fullpdf
Reference11 articles.
1. Substituent effects on the tautomer ratios between the hydrazone imine and diazenyl enamine forms in side-chained quinoxalines
2. Substituent effects on the tautomer ratios between the hydra-zone imine and diazenyl enamine forms in 3-(arylhydra-zono)methyl-2-oxo-1,2-dihydroquinoxalines. Correlation of the hammett constants σpwith the tautomeric equilibrium constants KT
3. Substituent and solvent effects on the tautomer ratios between the hydrazone imine and diazenyl enamine forms inp- andm-substituted 3-(arylhydrazono)methyl-2-oxo-1,2-dihydroquinoxalines
4. A selective synthesis of 1-aryl-3-quinoxalinyl-1,2,4-triazole and furo[2,3-b]quinoxaline
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