<?xml version="1.0"?>
<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=133746"><dc:title>Conformationally driven Ru(II)-catalyzed multiple ortho-C-H bond activation in diphenylpyrazine derivatives in water</dc:title><dc:creator>Hrovat,	Sara	(Avtor)
	</dc:creator><dc:creator>Drev,	Miha	(Avtor)
	</dc:creator><dc:creator>Grošelj,	Uroš	(Avtor)
	</dc:creator><dc:creator>Perdih,	Franc	(Avtor)
	</dc:creator><dc:creator>Svete,	Jurij	(Avtor)
	</dc:creator><dc:creator>Štefane,	Bogdan	(Avtor)
	</dc:creator><dc:creator>Požgan,	Franc	(Avtor)
	</dc:creator><dc:subject>ruthenium catalysts</dc:subject><dc:subject>heterocycles</dc:subject><dc:subject>green chemistry</dc:subject><dc:subject>microwave</dc:subject><dc:subject>direct arylation</dc:subject><dc:description>Ru(II)/carboxylate/PPh$_3$ catalyst system enabled the preparation of highly conjugated pyrazine derivatives in water under microwave irradiation. Both nitrogen atoms efficiently dictated cleavage of the ortho-C–H bonds in both benzene rings of 2,3-diphenylpyrazine substrates through chelation assistance. In conformationally more flexible diphenyldihydropyrazine 1, the arylation of four ortho-C–H bonds was possible, while in the aromatic analog 2, the triarylation was the limit.</dc:description><dc:date>2020</dc:date><dc:date>2021-12-13 14:07:01</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>133746</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
