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				<datestamp>2011-06-30T10:44:15Z</datestamp>
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	<dc:title xml:lang="en-US">Green methodologies in organic synthesis: Microwave assisted solvent- and catalyst-free synthesis of enaminones and their conversion into 1,3,5-trisubstituted benzenes as well as 3-aroyl-6-substituted pyridines</dc:title>
	<dc:creator>El-Apasery, Morsy Ahmed</dc:creator>
	<dc:creator>Al-Mousawi, Saleh Mohamed</dc:creator>
	<dc:creator>Elnagdi, Mohamed Helmy</dc:creator>
	<dc:subject xml:lang="en-US">Enaminone</dc:subject>
	<dc:subject xml:lang="en-US">Solvent-free</dc:subject>
	<dc:subject xml:lang="en-US">Green chemistry</dc:subject>
	<dc:subject xml:lang="en-US">Dye intermediates</dc:subject>
	<dc:subject xml:lang="en-US">Microwave irradiation</dc:subject>
	<dc:subject xml:lang="en-US">1</dc:subject>
	<dc:subject xml:lang="en-US">3</dc:subject>
	<dc:subject xml:lang="en-US">5-trisubstituted benzenes</dc:subject>
	<dc:description xml:lang="en-US">Enaminones were obtained in good yields via condensing methyl ketones with (N,N-dimethylformamide dimethyl acetal) DMF-DMA under microwave irradiation in absence of solvent. These enaminones were readily converted into 1,3,5-trisubstituted benzenes. Reacting enaminones in presence of ammonium acetate has afforded pyridine derivatives.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2011-06-30</dc:date>
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	<dc:identifier>10.5155/eurjchem.2.2.168-172.228</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 2 No. 2 (2011): June 2011; 168-172</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
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