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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://dk.um.si/IzpisGradiva.php?id=27012"><dc:title>PolyHIPE supports in batch and flow-through Suzuki cross-coupling reactions</dc:title><dc:creator>Brown,	Jane F.	(Avtor)
	</dc:creator><dc:creator>Krajnc,	Peter	(Avtor)
	</dc:creator><dc:creator>Cameron,	Neil R.	(Avtor)
	</dc:creator><dc:subject>polymer supports</dc:subject><dc:subject>polymer monoliths</dc:subject><dc:subject>emulsion polymerisation</dc:subject><dc:subject>solid-phase synthesis</dc:subject><dc:subject>cross-coupling reactions</dc:subject><dc:description>As part of ongoing research efforts to discover alternative support materials to polymer beads for use in polymer-supported synthesis, particularly under flow-through conditions, this work involves the synthesis of PolyHIPE (High Internal Phase Emulsion) polymer monoliths. PolyHIPEs containing high loadings of chloromethyl groups were efficiently prepared by the direct copolymerization of 4-vinylbenzyl chloride and divinylbenzene monomers. The 'Merrifield' PolyHIPE proved to be an excellent support for batch and flow-through Suzuki cross-coupling reactions. A remarkably high yield of pure biaryl product was obtained using the PolyHIPE support in cubic form and utilizing an electron-rich boronic acid. In comparison to polymer beads, this material was found to be a much more efficient support in both batch and continuous flow modes. PolyHIPE converted a greater amount of chloromethyl groups into biaryl product under identical reaction conditions. It is suggested that the absence of channelling with PolyHIPE monoliths gives better performance under flow-through conditions than permanently porous beads.</dc:description><dc:date>2005</dc:date><dc:date>2012-06-01 09:37:39</dc:date><dc:type>Neznano</dc:type><dc:identifier>27012</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
