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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=154836"><dc:title>Catalytic performance of Noyori–Ikariya-type ruthenium complex with tethered syn-ULTAM ligand for the asymmetric transfer hydrogenation of ketones</dc:title><dc:creator>Hašanová,	Simona	(Avtor)
	</dc:creator><dc:creator>Cingl,	Jernej	(Avtor)
	</dc:creator><dc:creator>Tomašič,	Tihomir	(Avtor)
	</dc:creator><dc:creator>Cotman,	Andrej Emanuel	(Avtor)
	</dc:creator><dc:subject>asymmetric synthesis</dc:subject><dc:subject>ruthenium</dc:subject><dc:subject>hydrogenation</dc:subject><dc:subject>alcohol</dc:subject><dc:description>The ruthenium complex of the tethered syn-ULTAM ligand, i.e. syn-3-(α-aminobenzyl)-benzo-γ-sultam, has been evaluated for the asymmetric transfer hydrogenation (ATH) of a variety of ketones in formic acid/triethylamine mixture. Its performance was similar to the established Noyori–Ikariya-type catalysts for the reduction of benzo-fused cyclic ketones, but the enantioselectivity for the reduction of acetophenone was only moderate. The syn-ULTAM-based catalyst was particularly efficient and enantioselective for ATH of the sterically demanding α,α-disubstituted ketones. Moreover, we report a divergent ATH of 2-phenyl-1,3-indandione to either cis-2-phenyl-1-indanol, or cis,trans-2-phenyl-1,3-indandiol.</dc:description><dc:date>2024</dc:date><dc:date>2024-03-05 12:45:17</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>154836</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
