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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>One-pot synthesis and photochemical diversification of pyrazolo[1,2-a]pyridazinones into 3D-rich scaffolds</dc:title><dc:creator>Babnik,	Ines	(Avtor)
	</dc:creator><dc:creator>Petek,	Nejc	(Avtor)
	</dc:creator><dc:creator>Grošelj,	Uroš	(Avtor)
	</dc:creator><dc:creator>Svete,	Jurij	(Avtor)
	</dc:creator><dc:creator>Štefane,	Bogdan	(Avtor)
	</dc:creator><dc:subject>atmospheric chemistry</dc:subject><dc:subject>azomethine</dc:subject><dc:subject>cyclization</dc:subject><dc:subject>irradiation</dc:subject><dc:subject>reaction products</dc:subject><dc:description>We report a one-pot, three-component synthesis of pyrazolo[1,2-a]pyridazinones from tetrahydropyridazines, a transformation that was historically challenging due to competing ring contractions. The resulting compounds undergo photoinduced transformations, without the need for external photocatalysts, to afford diverse 3D-rich derivatives, including tricyclic cyclobutenes and γ-(pyrazol-1-yl)butanals. Enabled by mild conditions, this strategy offers an efficient, atom-economical route to structurally diverse pyrazolo[1,2-a]pyridazinones and their derivatives.</dc:description><dc:date>2026</dc:date><dc:date>2026-02-19 12:17:37</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>179667</dc:identifier><dc:identifier>UDK: 547.8:544.52</dc:identifier><dc:identifier>ISSN pri članku: 0022-3263</dc:identifier><dc:identifier>DOI: 10.1021/acs.joc.5c02313</dc:identifier><dc:identifier>COBISS_ID: 268035331</dc:identifier><dc:language>sl</dc:language></metadata>
