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				<datestamp>2012-12-31T23:10:35Z</datestamp>
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	<dc:title xml:lang="en-US">Selective iodination of 2-acetyl-1-naphthol using iodine and iodic acid  under solvent-free grinding technique</dc:title>
	<dc:creator>Zangade, Sainath</dc:creator>
	<dc:creator>Mokle, Shyam</dc:creator>
	<dc:creator>Shinde, Avinash</dc:creator>
	<dc:creator>Vibhute, Yeshwant</dc:creator>
	<dc:subject xml:lang="en-US">Iodine</dc:subject>
	<dc:subject xml:lang="en-US">Iodic acid</dc:subject>
	<dc:subject xml:lang="en-US">Solvent-free</dc:subject>
	<dc:subject xml:lang="en-US">Grinding technique</dc:subject>
	<dc:subject xml:lang="en-US">Selective iodination</dc:subject>
	<dc:subject xml:lang="en-US">2-Acetyl-1-naphthol</dc:subject>
	<dc:description xml:lang="en-US">Selective electrophilic iodination of 2-acetyl-1-naphthol was achieved using iodine and iodic acid in combination with grinding at room temperature under solvent-free conditions to yield 1-(1-hydroxy-4-iodo-naphthalen-2-yl)-ethanone. Grinding mode of reactions has not only of interest from economical point of view, in many cases they also offer considerable advantages in terms of yield, mild reaction  conditions, selectivity and simplicity of reaction procedure.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2012-09-30</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/641</dc:identifier>
	<dc:identifier>10.5155/eurjchem.3.3.314-315.641</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 3 No. 3 (2012): September 2012; 314-315</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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