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Pyran and Pyridine as Building Blocks in Heterocyclic Synthesis
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 Title & Authors
Pyran and Pyridine as Building Blocks in Heterocyclic Synthesis
El-Hashash, Maher.A.; El-Sawy, Abdallah.A.; Eissa, Abdelmonem.M.F.;
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 Abstract
The present work is devoted to study the interaction of -aroylacrylic acid derivative (3) with malononitrile in (DMF) in the presence of piperidine and/or ammonium acetate, then using the formed compounds as starting materials for synthesizing fused and isolated heterocyclic systems. It has been established that the -aroylacrylic acid (3) reacts with malononitrile in (DMF) in the presence of piperidine as a catalyst with the formation of 4H-pyran derivative (4). By changing the catalyst into ammonium acetate, pyridine derivative (5) has been obtained. Also the N-maleamic acid derivatives (19) and (27) have been synthesized via the interaction of (4) and (5) with maleic anhydride. The purpose of this step is to study the behavior of the formed maleamic acid derivatives – as analogies of -aroylacrylic acids – towards different active methylene compounds under Michael addition reaction.
 Keywords
-Aroylacrylic acid;Michael reaction;2-aminopyran;2-aminopyridine;Pyrimidine;Maleamic-acid;
 Language
Korean
 Cited by
1.
Ultrasonic and Grinding Aptitudes of One-Pot Synthesis of 5-(4-Chlorophenyl)-7-(3,4-Dimethyl Phenyl)-2-oxo-2H-Pyrano[2,3-b]Pyridine Derivatives as Antibacterial Agents, Journal of Heterocyclic Chemistry, 2017, 54, 3, 2003  crossref(new windwow)
2.
Synthesis of Novel Spiro Pyrano[2,3-d]thiazolo[3,2-a]pyrimidine via 1,3-Dipolar Cycloaddition of Azomethine Ylide, Journal of Heterocyclic Chemistry, 2013, n/a  crossref(new windwow)
3.
Behaviour of 4-[4-methoxy-3-methylphenyl]-4-oxobutenoic acid towards nitrogen-containing nucleophiles, Journal of Chemical Sciences, 2014, 126, 6, 1883  crossref(new windwow)
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