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	<dc:title xml:lang="en-US">Synthesis of some novel benzimidazole derivatives and their biological evaluation</dc:title>
	<dc:creator>Gund, Dnyandev Radhu</dc:creator>
	<dc:creator>Rao, Balivada Venkata Satyasai Varaprasad</dc:creator>
	<dc:creator>Mandhare, Pandurang Narayanrao</dc:creator>
	<dc:creator>Vaidya, Sanjay Dashrath</dc:creator>
	<dc:subject xml:lang="en-US">Alkylation</dc:subject>
	<dc:subject xml:lang="en-US">Benzimidazole</dc:subject>
	<dc:subject xml:lang="en-US">Suzuki coupling</dc:subject>
	<dc:subject xml:lang="en-US">Antifungal activity</dc:subject>
	<dc:subject xml:lang="en-US">Phenyl boronic acid</dc:subject>
	<dc:subject xml:lang="en-US">Antibacterial activity</dc:subject>
	<dc:description xml:lang="en-US">A series of novel benzimidazole derivatives have been synthesized by the condensation of o-phenylenediamine with 4-bromophenoxy acetic acid and product obtained was alkylated at the benzimidazole -NH with different electrophilic reagents. Subsequent reactions of the products by the Suzuki Coupling between benzimidazole derivatives and phenylboronic acid derivatives were accomplished. All these compounds were characterized by FT-IR, 1H NMR, MS and elemental analysis. These compounds were screened for their potential antibacterial and antifungal activities. This exhibited some promising results towards testing organism in-vitro.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2015-09-30</dc:date>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/1242</dc:identifier>
	<dc:identifier>10.5155/eurjchem.6.3.270-274.1242</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 6 No. 3 (2015): September 2015; 270-274</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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