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	<dc:title xml:lang="en-US">Synthesis of some novel pyridine and naphthyridine derivatives</dc:title>
	<dc:creator>Abdelrazek, Fathy Mohamed</dc:creator>
	<dc:creator>Kassab, Nazmi Abdel-Latif</dc:creator>
	<dc:creator>Metwally, Nadia Hanafy</dc:creator>
	<dc:creator>Sobhy, Nehal Ahmed</dc:creator>
	<dc:subject xml:lang="en-US">Fur-2-ylethylidenemalononitrile</dc:subject>
	<dc:subject xml:lang="en-US">Thien-2-ylethylidenemalononitrile</dc:subject>
	<dc:subject xml:lang="en-US">Dihydro-pyridines</dc:subject>
	<dc:subject xml:lang="en-US">Pyrazolo-naphthyridines</dc:subject>
	<dc:subject xml:lang="en-US">Pyrimido-naphthyridines</dc:subject>
	<dc:description xml:lang="en-US">2-[1-(Furan- or thiophen-2-yl)ethylidene)malononitriles (1a,b) undergo dimerization reactions in ethanol catalyzed by sodium ethoxide to afford 2-[4,6-di(furan- or thiophen-2-yl)-3-cyano-6-methyl-5,6-dihydropyridin-2(1H)-ylidene]malononitrile derivatives (2a,b), respectively. Compounds 2a and 2b couple with arene diazonium salts (3a-c) to afford the hydrazo derivatives (4a-f). They react also with hydrazines (5a,b) to afford the pyrazolo[3,4-H][1,6]naphthyridine derivatives (6a-d) and with urea derivatives (7a-c) to afford the pyrimido[4,5-H][1,6]naphthyridine derivatives (8a-f), respectively.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2010-12-22</dc:date>
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	<dc:identifier>10.5155/eurjchem.1.4.368-372.104</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 1 No. 4 (2010): December 2010; 368-372</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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