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	<dc:title xml:lang="en-US">Microwave assisted synthesis of 2-amino-6-methoxy-4H-benzo[h]chromene derivatives</dc:title>
	<dc:creator>El-Agrody, Ahmed Mohamed</dc:creator>
	<dc:creator>Al-Dies, Al-Anood Mohamed</dc:creator>
	<dc:creator>Fouda, Ahmed Mahmoud</dc:creator>
	<dc:subject xml:lang="en-US">Benzochromenes</dc:subject>
	<dc:subject xml:lang="en-US">Pyran derivatives</dc:subject>
	<dc:subject xml:lang="en-US">Microwave synthesis</dc:subject>
	<dc:subject xml:lang="en-US">4-Methoxy-1-naphthol</dc:subject>
	<dc:subject xml:lang="en-US">α-Cyanocinnamonitriles</dc:subject>
	<dc:subject xml:lang="en-US">Ethyl α-cyanocinnamates</dc:subject>
	<dc:description xml:lang="en-US">A convenient and efficient method using microwave assisted synthesis of 4H-benzo[h]chromenes (7 and 8), by the reaction of 4-methoxy-1-naphthol (1) with a mixture of aromatic aldehydes (2) and malononitrile (3) or ethyl cyanoacetate (5) and also, by the reaction of 4-methoxy-1-naphthol (1) with α-cyanocinnamonitriles (4) or ethyl α-cyanocinnamates (6) in ethanolic piperidine solution was examined. Structures of the newly synthesized compounds were established on the basis of spectral data, IR, 1H NMR, 13C NMR, 13C NMR-DEPT and MS data.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2014-03-31</dc:date>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/923</dc:identifier>
	<dc:identifier>10.5155/eurjchem.5.1.133-137.923</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 5 No. 1 (2014): March 2014; 133-137</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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