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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=180678"><dc:title>HAT-initiated fragmentation of 4-(dimethylamino)-1-((3-methylbut-2-en-1-yl)oxy)-3-phenylbut-3-en-2-one</dc:title><dc:creator>Bogataj,	Andrej	(Avtor)
	</dc:creator><dc:creator>Ciber,	Luka	(Avtor)
	</dc:creator><dc:creator>Petek,	Nejc	(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>alkene</dc:subject><dc:subject>enaminone</dc:subject><dc:subject>hydrogen atom transfer</dc:subject><dc:subject>fragmentation</dc:subject><dc:subject>tetrabutylammonium decatungstate</dc:subject><dc:subject>phenylacetone</dc:subject><dc:description>An alkene-tethered enaminone 7 was synthesized in four steps from bromoacetic acid and 3,3-dimethylallyl alcohol. The enaminone was fully characterized, including UV-Vis spectra. TBADT-catalyzed HAT of the alkene-tethered enaminone initiated a fragmentation that yielded the literature-known phenylacetone-derived enaminone.
</dc:description><dc:date>2026</dc:date><dc:date>2026-03-13 12:23:49</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>180678</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>