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dc.contributor.authorGuo, Kai
dc.contributor.authorThompson, Mark J.
dc.contributor.authorReddy, Tummala Rama Krishna
dc.contributor.authorMutter , Roger
dc.contributor.authorChen, Beining
dc.date.accessioned2013-09-17T09:45:17Z
dc.date.available2013-09-17T09:45:17Z
dc.date.issued2007-06-11
dc.identifier.citationGuo , K , Thompson , M J , Reddy , T R K , Mutter , R & Chen , B 2007 , ' Mechanistic studies leading to a new procedure for rapid microwave assisted generation of pyridine-3,5-dicarbonitrile libraries ' , Tetrahedron , vol. 63 , no. 24 , pp. 5300-11 . https://doi.org/10.1016/j.tet.2007.03.139
dc.identifier.urihttp://hdl.handle.net/2299/11596
dc.description.abstractMechanistic investigations into the multi-component synthesis of pyridine-3,5-dicarbonitriles have established a defined reaction pathway, particularly clarifying the role of aerobic oxidation in conversion of the intermediate 1,4-dihydropyridines into the final products. Based on such improved understanding of the reaction mechanism, optimised conditions for the preparation of compound libraries based on this core structure have been developed and represent a significant improvement in yield over existing protocols. Particularly, microwave assisted synthesis was found to provide a procedure suitable for high-throughput synthesis of pyridine-3,5-dicarbonitrile libraries.en
dc.format.extent381636
dc.language.isoeng
dc.relation.ispartofTetrahedron
dc.titleMechanistic studies leading to a new procedure for rapid microwave assisted generation of pyridine-3,5-dicarbonitrile librariesen
dc.contributor.institutionDepartment of Pharmacy
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionHealth & Human Sciences Research Institute
dc.contributor.institutionMedicinal and Analytical Chemistry
dc.description.statusPeer reviewed
rioxxterms.versionofrecord10.1016/j.tet.2007.03.139
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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