Simple,One-Pot,and Three-Component Coupling Reactions of Azaarenes (Phenanthridine,Isoquinoline, and Quinoline), with Acetylenic Esters Involving Methyl Propiolate or Ethyl Propiolate in the Presence of NH-Heterocyclic or 1,3-Dicarbonyl Compounds |
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Authors: | Mahmoud Nassiri |
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Affiliation: | 1. Faculty of Marine Science , Chabahar Maritime University , Chabahar , Iran mdnassiri@yahoo.com |
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Abstract: | Three-component reactions involving azaarenes (quinoline, isoquinoline, and phenanthridine) with acetylenic esters such as methyl propiolate or ethyl propiolate in the presence of NH-heterocyclic compounds (carbazole, maleimide, 5-nitroindazole, 2-benzoxazolinone, indole, and 2-methylindole) or 1,3-dicarbonyl compounds involving acetylacetone and N,N′-dimethylbar bituric acid are described. The reactions proceeded smoothly at room temperature without a catalyst and with excellent yields. This method is very useful for functionalizing aza-aromatic compounds in a one-pot operation. |
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Keywords: | Azaarenes 1,3-dicarbonyl compounds enamino esters ethyl propiolate methyl propiolate NH-heterocyclic compounds |
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