Substituent effects on the tautomer ratios between the hydrazone imine and diazenyl enamine forms in side-chained quinoxalines
Author:
Publisher
Wiley
Subject
Organic Chemistry
Reference14 articles.
1. NMR study on the tautomeric equilibria between the hydrazone imine and diazenyl enamine forms in side chained quinoxalines: Solvent effects and temperature dependence
2. Synthesis of novel 3-(α-arylhydrazono-1,3,4-oxadiazol-2-ylmethyl)-2-oxo-1,2-dihydroquinoxalines and their characteristic tautomerism between the hydrazone imine and diazenyl enamine forms
3. Tautomeric behavior of 3-(α-arylhydrazono)methyl-2-oxo-1,2-dihydroquinoxalines between hydrazone imine and diazenyl enamine forms
4. A convenient synthesis of 3-formyl-2-oxo-1,2-dihydroquinoxaline chlorophenylhydrazones: Novel tautomeric equilibria between hydrazone imine and diazenyl enamine forms with long-range pSSrototropy
5. A convenient synthesis and antifungal activity of 1-aryl-1H- and 1-aryl-3-heteroaryl-1H-pyrazolo[3,4-b]quinoxalinesA Convenient Synthesis and Antifungal Activity
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