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	<dc:title xml:lang="en-US">Synthesis and bioactivity of phosphorylated derivatives of stavudine</dc:title>
	<dc:creator>Rao, Alahari Janardhan</dc:creator>
	<dc:creator>Rao, Valasani Koteswara</dc:creator>
	<dc:creator>Rao, Pasupuleti Visweswara</dc:creator>
	<dc:creator>Raju, Chamarthi Naga</dc:creator>
	<dc:creator>Ghosh, Sunil Kumar</dc:creator>
	<dc:subject xml:lang="en-US">Phosphorylated derivatives of stavudine</dc:subject>
	<dc:subject xml:lang="en-US">Gram-positive bacteria</dc:subject>
	<dc:subject xml:lang="en-US">Gram-negative bacteria</dc:subject>
	<dc:subject xml:lang="en-US">Antibacterial activity</dc:subject>
	<dc:subject xml:lang="en-US">Antioxidant activity</dc:subject>
	<dc:description xml:lang="en-US">Novel phosphorylated derivatives of stavudine were synthesized by the reaction of bis(2-chloroethyl)phosphoramidic dichloride/4-nitrophenyl phosphorodichloridate with various cyclic amines and amino acid esters in the presence of triethylamine in dry tetrahydrofuran through the corresponding monochloride intermediates 2a-l. Further reaction of the intermediates 2a-l with stavudine in tetrahydrofuran and pyridine in the presence of triethylamine formed the title compounds 4a-l. Their structures were characterized by IR,   1H-, 13C-, 31P-NMR and mass spectral data analyses. They exhibited good antibacterial and antioxidant activities. Their bioactivity was greatly influenced by the different groups present at the phosphorus.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2010-12-22</dc:date>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/20</dc:identifier>
	<dc:identifier>10.5155/eurjchem.1.4.297-301.20</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 1 No. 4 (2010): December 2010; 297-301</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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