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	<dc:title xml:lang="en-US">1,2,4-Triazine Chemistry Part I: Orientation of cyclization reactions of functionalized 1,2,4-triazine derivatives</dc:title>
	<dc:creator>Abdel-Rahman, Reda Mohammady</dc:creator>
	<dc:creator>Makki, Mohammed Saleh Tawfik</dc:creator>
	<dc:creator>Ali, Tarik El-Sayed</dc:creator>
	<dc:creator>Ibrahim, Magdy Ahmed</dc:creator>
	<dc:subject xml:lang="en-US">1</dc:subject>
	<dc:subject xml:lang="en-US">2</dc:subject>
	<dc:subject xml:lang="en-US">4-Triazines</dc:subject>
	<dc:subject xml:lang="en-US">Chemical reactivity</dc:subject>
	<dc:subject xml:lang="en-US">Cyclization reactions</dc:subject>
	<dc:description xml:lang="en-US">Orientation of heterocyclization reactions of functionalized 1,2,4-triazines were studied by effect of substituents in 1,2,4-triazine moieties, type of the solvent used in the reaction and the temperature effect. Also, it was found that cyclization process depended mainly on the chemoselective and regioselectivity states of the parent substrate as well as preferring cite of ring closure.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2010-09-29</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/54</dc:identifier>
	<dc:identifier>10.5155/eurjchem.1.3.236-245.54</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 1 No. 3 (2010): September 2010; 236-245</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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