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				<datestamp>2011-04-06T06:10:52Z</datestamp>
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	<dc:title xml:lang="en-US">Synthesis of 8-hydroxy-6-methoxy-3-pentyl-1H-isochromen-1-one from Tessmannia densiflora</dc:title>
	<dc:creator>Saeed, Aamer</dc:creator>
	<dc:subject xml:lang="en-US">Isocoumarin</dc:subject>
	<dc:subject xml:lang="en-US">Tessmannia densiflora</dc:subject>
	<dc:subject xml:lang="en-US">3</dc:subject>
	<dc:subject xml:lang="en-US">5-Dimethoxyhomophthalic acid</dc:subject>
	<dc:subject xml:lang="en-US">Antimalarial</dc:subject>
	<dc:subject xml:lang="en-US">5-Dimethoxyhomophthalic anhydride</dc:subject>
	<dc:subject xml:lang="en-US">Mechanism</dc:subject>
	<dc:description xml:lang="en-US">The synthesis of 8-hydroxy-6-methoxy-3-pentyl-1H-isochromen-1-one (1) isolated from the stem and root bark extracts of Tessmannia densiflora has been described. The reaction of 3,5-dimethoxyhomophthalic anhydride (2) with hexanoyl chloride in the presence of 1,1,3,3-tetramethylguanidine and triethylamine afforded 6,8-dimethoxy-3-pentylisocoumarin (3). Regioselective demethylation of the latter using anhydrous aluminum chloride furnished the title isocoumarin (1).</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2011-03-28</dc:date>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/201</dc:identifier>
	<dc:identifier>10.5155/eurjchem.2.1.117-119.201</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 2 No. 1 (2011): March 2011; 117-119</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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