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	<dc:title xml:lang="en-US">Zinc dust: An extremely active and reusable catalyst in acylation of phenols, thiophenol, amines and alcohols in a solvent-free system</dc:title>
	<dc:creator>Pasha, Mohamed Afzal</dc:creator>
	<dc:creator>Reddy, Muthukur Bhojegowd Madhusudana</dc:creator>
	<dc:creator>Manjula, Krishnappa</dc:creator>
	<dc:subject xml:lang="en-US">Zinc dust</dc:subject>
	<dc:subject xml:lang="en-US">Phenols</dc:subject>
	<dc:subject xml:lang="en-US">Thiophenol</dc:subject>
	<dc:subject xml:lang="en-US">Amines</dc:subject>
	<dc:subject xml:lang="en-US">Acyl chloride</dc:subject>
	<dc:subject xml:lang="en-US">Solvent-Free condition</dc:subject>
	<dc:description xml:lang="en-US">A trace amount of zinc dust is able to promote instantaneous quantitative acylation of a large variety of functionalized phenols, thiophenol, amines and alcohols with acyl chlorides under solvent-free condition at 25 °C. The catalyst can be recovered and recycled making the procedure potentially useful for industrial applications.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2010-12-23</dc:date>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/90</dc:identifier>
	<dc:identifier>10.5155/eurjchem.1.4.385-387.90</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 1 No. 4 (2010): December 2010; 385-387</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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