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									<identifier>oai:www.peertechzpublications.org:10.17352/abse.000009</identifier>
									<datestamp>2018-12-21</datestamp>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										Microwave Irradiated and Conventional Synthesis, Antibacterial Activity Evaluation Studies of Tryptamine-Azole-Fluoroquinolone Conjugates
										</dc:title><dc:creator>Yıldız Uygun Cebeci1</dc:creator><dc:creator> Serap Basoglu Özdemir1</dc:creator><dc:creator> Ahmet Demirbas1</dc:creator><dc:creator> Neslihan Demirbas</dc:creator><dc:creator>Sengül Alpay Karaoglu</dc:creator><dc:description>&lt;p&gt;Tryptamine was converted to the corresponding 1,2,4-triazole, 1,3,4-oxadiazole, 5-oxo-1,3-thia(oxa)zolidine and 5-(4-chlorophenyl)-1,3-thia(oxa)zole derivatives via several steps. 1,3,4-oxadiazole and 1,2,4-triazoles were then converted to the corresponding Mannich bases containing fluroquinolone core using a one-pot three-components procedure. Conventional and microwave-assisted methods were applied for all syntheses. All the newly synthesized compounds were screened for their antibacterial and most of them were found to have good–moderate antibacterial activity.&lt;/p&gt;</dc:description>
										<dc:publisher>Archive of Biomedical Science and Engineering - Peertechz Publications</dc:publisher>
										<dc:date>2018-12-21</dc:date>
										<dc:type>Research Article</dc:type>
										<dc:identifier>https://doi.org/10.17352/abse.000009</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Yıldız Uygun Cebeci1 et al.</dc:rights>
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