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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=152885"><dc:title>Synthesis of six-membered N-heterocyclic carbene precursors based on camphor</dc:title><dc:creator>Šegina,	Jan	(Avtor)
	</dc:creator><dc:creator>Ciber,	Luka	(Avtor)
	</dc:creator><dc:creator>Brodnik,	Helena	(Avtor)
	</dc:creator><dc:creator>Požgan,	Franc	(Avtor)
	</dc:creator><dc:creator>Svete,	Jurij	(Avtor)
	</dc:creator><dc:creator>Štefane,	Bogdan	(Avtor)
	</dc:creator><dc:creator>Grošelj,	Uroš	(Avtor)
	</dc:creator><dc:subject>ketopinic acid</dc:subject><dc:subject>amidation</dc:subject><dc:subject>reduction</dc:subject><dc:subject>diamines</dc:subject><dc:subject>N-heterocyclic carbene precursors</dc:subject><dc:subject>asymmetric catalysis</dc:subject><dc:subject>amidinium salts</dc:subject><dc:subject>hydrolysis</dc:subject><dc:description>The endo- and exo-N-heterocyclic carbene precursors based on camphor were prepared
diastereoselectively in five synthetic steps starting from (1S)-(+)-ketopinic acid. The obtained Nheterocyclic carbene precursors were investigated in an asymmetric benzoin reaction. All newcompounds were fully characterized, and the absolute configurations were determined via X-ray diffraction and NOESY measurements.</dc:description><dc:date>2023</dc:date><dc:date>2023-12-11 09:22:25</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>152885</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>