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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://repozitorij.uni-lj.si/IzpisGradiva.php?id=129624"><dc:title>Copper(I)-catalyzed [3 + 2] cycloaddition of 3-azidoquinoline-2,4(1H,3H)-diones with terminal alkynes</dc:title><dc:creator>Kafka,	Stanislav	(Avtor)
	</dc:creator><dc:creator>Hauke,	Sylvia	(Avtor)
	</dc:creator><dc:creator>Salčinović,	Arjana	(Avtor)
	</dc:creator><dc:creator>Soidinsalo,	Otto	(Avtor)
	</dc:creator><dc:creator>Urankar,	Damijana	(Avtor)
	</dc:creator><dc:creator>Košmrlj,	Janez	(Avtor)
	</dc:creator><dc:subject>cycloaddition</dc:subject><dc:subject>azides</dc:subject><dc:subject>quinoline-2</dc:subject><dc:subject>4(1H</dc:subject><dc:subject>3H)-diones</dc:subject><dc:subject>terminal alkynes</dc:subject><dc:subject>1</dc:subject><dc:subject>2</dc:subject><dc:subject>3-triazoles</dc:subject><dc:description>3-Azidoquinoline-2,4(1H,3H)-diones 1, which are readily available from 4-hydroxyquinolin-2(1H)-ones 4 via 3-chloroquinoline-2,4(1H,3H)-diones 5, afford, in copper(I)-catalyzed [3 + 2] cycloaddition reaction with terminal acetylenes, 1,4-disubstituted 1,2,3-triazoles 3 in moderate to excellent yields. The structures of compounds 3 were confirmed by $^1$H and $^{13}$C-NMR spectroscopy, combustion analyses and mass spectrometry.</dc:description><dc:date>2011</dc:date><dc:date>2021-09-06 09:38:20</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>129624</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
