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				<datestamp>2018-09-30T08:12:27Z</datestamp>
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	<dc:title xml:lang="en-US">Microwave assisted one pot conversion of aromatic aldehydes to nitriles</dc:title>
	<dc:creator>Hijji, Yousef Mohammad</dc:creator>
	<dc:creator>Rajan, Rajeesha</dc:creator>
	<dc:creator>Tabba, Hani Darwish</dc:creator>
	<dc:creator>Abu-Yousef, Imad Ali</dc:creator>
	<dc:creator>Mansour, Said</dc:creator>
	<dc:creator>Yahia, Hamdi Ben</dc:creator>
	<dc:subject xml:lang="en-US">Aldoxime</dc:subject>
	<dc:subject xml:lang="en-US">Aldehyde</dc:subject>
	<dc:subject xml:lang="en-US">Aryl nitrile</dc:subject>
	<dc:subject xml:lang="en-US">Microwave</dc:subject>
	<dc:subject xml:lang="en-US">Elimination</dc:subject>
	<dc:subject xml:lang="en-US">Hydroxylamine</dc:subject>
	<dc:description xml:lang="en-US">Nitriles are versatile organic precursors in organic synthesis and have numerous applications. An efficient microwave assisted method for conversion of aromatic aldehydes to the corresponding nitriles is reported. Aldehydes are readily converted to oxime followed by acetylation and acetic acid elimination to provide nitriles in good yields within minutes. The method proved to be efficient for the synthesis of aromatic and heterocyclic nitriles. The reaction proceeds smoothly by microwave at 150 °C for 5 minutes. The obtained products are isolated simply by filtration or extraction.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2018-09-30</dc:date>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/1751</dc:identifier>
	<dc:identifier>10.5155/eurjchem.9.3.269-274.1751</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 9 No. 3 (2018): September 2018; 269-274</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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	<dc:rights xml:lang="en-US">Copyright (c) 2018 Authors</dc:rights>
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