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				<datestamp>2013-06-30T03:41:05Z</datestamp>
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	<dc:title xml:lang="en-US">An efficient synthesis of some new isolated and fused 2-oxo-2H-chromene derivatives as antimicrobial and antitumor agents</dc:title>
	<dc:creator>El-Shaaer, Hafez Mohamed</dc:creator>
	<dc:subject xml:lang="en-US">Synthesis</dc:subject>
	<dc:subject xml:lang="en-US">Antitumor activity</dc:subject>
	<dc:subject xml:lang="en-US">Cyclocondensation</dc:subject>
	<dc:subject xml:lang="en-US">2-Oxo-2H-chromene</dc:subject>
	<dc:subject xml:lang="en-US">Antimicrobial Activity</dc:subject>
	<dc:subject xml:lang="en-US">Chromeno[3</dc:subject>
	<dc:subject xml:lang="en-US">4-c]pyridin-5-ones</dc:subject>
	<dc:description xml:lang="en-US">An efficient synthesis of the biologically active novel systems derived from the reaction of 4-methyl-2-oxo-2H-chromene-3-carbonitrile (1) with sodium hydroxide and/or DMF-DMA and cyclocondensation reactions of 4-[(E)-2-(dimethylamino)ethenyl]-2-oxo-2H-chromene-3-carbonitrile (5) with nitrogen nucleophilic reagents afforded the corresponding 4-iminochromeno[3,4-c]pyridine derivatives (6-14). The structures of the prepared compounds have been proved by elemental analysis, IR, 1H  and 13C NMR and mass spectra. Significant antitumor activities in planta were observed for some of the prepared compounds.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2013-06-30</dc:date>
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	<dc:identifier>10.5155/eurjchem.4.2.138-145.749</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 4 No. 2 (2013): June 2013; 138-145</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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