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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=125378"><dc:title>Designing homogeneous copper-free Sonogashira reaction through a prism of Pd-Pd transmetalation</dc:title><dc:creator>Martek,	Bruno Aleksander	(Avtor)
	</dc:creator><dc:creator>Gazvoda,	Martin	(Avtor)
	</dc:creator><dc:creator>Urankar,	Damijana	(Avtor)
	</dc:creator><dc:creator>Košmrlj,	Janez	(Avtor)
	</dc:creator><dc:subject>catalysis</dc:subject><dc:subject>palladium</dc:subject><dc:subject>Sonogashira reaction</dc:subject><dc:subject>alkyne</dc:subject><dc:subject>hydrocarbons</dc:subject><dc:subject>copper</dc:subject><dc:subject>ligands</dc:subject><dc:subject>addition reactions</dc:subject><dc:description>Simultaneous introduction of two different palladium (pre)catalysts, one tuned to promote oxidative addition to (hetero)aryl bromide and another to activate terminal alkyne substrate, leads to productive Pd−Pd transmetalation, subsequent reductive elimination, and formation of disubstituted alkyne. This conceptually novel rational design of copper-free Sonogashira reaction enabled facile identification of the reaction conditions, suitable for the synthesis of alkyl, aryl, and heteroaryl substituted alkynes at room temperature with as low as 0.125 mol % total Pd loading.</dc:description><dc:date>2020</dc:date><dc:date>2021-03-12 14:37:08</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>125378</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
