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4-(N-Boc-amino)-1,2,3-triazole-5-carbaldehydes upon heating under reflux in acetic acid in the presence of pyrrolidine react with cycloalkanones, acetylacetone, 1,3-cyclohexanediones, and malononitrile resulting in annulation of the pyridine ring with the formation… Click to show full abstract
4-(N-Boc-amino)-1,2,3-triazole-5-carbaldehydes upon heating under reflux in acetic acid in the presence of pyrrolidine react with cycloalkanones, acetylacetone, 1,3-cyclohexanediones, and malononitrile resulting in annulation of the pyridine ring with the formation of new derivatives of [1,2,3]triazolo[4,5-b]pyridine.
Keywords:
efficient method;
carboannulated functionalized;
triazolo pyridines;
method accessing;
functionalized triazolo;
accessing carboannulated
Journal Title: Chemistry of Heterocyclic Compounds
Year Published: 2020
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Journal Title: Chemistry of Heterocyclic Compounds
Year Published: 2020
Link to full text (if available)
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recommendations!