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				<datestamp>2011-06-30T10:44:15Z</datestamp>
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	<dc:title xml:lang="en-US">An improved synthesis of the alkaloid Luotonin-A employing ionic liquid and water as key solvents</dc:title>
	<dc:creator>Potewar, Taterao Marutao</dc:creator>
	<dc:creator>Kathiravan, Muthu Kumaradoss</dc:creator>
	<dc:creator>Chothe, Aparna Surendra</dc:creator>
	<dc:creator>Srinivasan, Kumar Venkatram</dc:creator>
	<dc:subject xml:lang="en-US">Ionic liquids</dc:subject>
	<dc:subject xml:lang="en-US">Luotonin A</dc:subject>
	<dc:subject xml:lang="en-US">Water</dc:subject>
	<dc:subject xml:lang="en-US">Pyrroloquinazoline</dc:subject>
	<dc:subject xml:lang="en-US">Volatile organic compounds</dc:subject>
	<dc:subject xml:lang="en-US">Anticancer activity</dc:subject>
	<dc:description xml:lang="en-US">Luotonin A is among the first known natural product possessing the heteroaromatic pyrroloquinazoline ring system. Although many syntheses have been reported for this compound, but they all have one or the other draw back such as a large number of steps, use of hazardous reagents like sodium hydride, low temperature reactions, and lengthy reaction time. Herein we report the synthesis of luotonin A achieved in five steps in which, two of the steps involved green solvents such as an ionic liquid and water as reaction media. In particular, we have achieved the reaction steps 1 and 3 involving the green solvents in much shorter reaction time than hitherto reported.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2011-06-30</dc:date>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/205</dc:identifier>
	<dc:identifier>10.5155/eurjchem.2.2.235-237.205</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 2 No. 2 (2011): June 2011; 235-237</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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