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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/34854
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dc.contributor.authorZaman, S.-
dc.contributor.authorMitsuru, K.-
dc.contributor.authorAbell, A.-
dc.date.issued2005-
dc.identifier.citationOrganic Letters, 2005; 7(4):609-611-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttp://hdl.handle.net/2440/34854-
dc.descriptionCopyright © 2005 American Chemical Society-
dc.description.abstract1-Benzyl-4-methylimidazoles with a range of substituents at the 2-position are prepared from O-pentafluorobenzoylamidoximes on treatment with catalytic amounts of Pd(PPh₃)₄ and triethylamine. The sequence provides access to optically active amino acid mimetics with a C-terminal imidazole.-
dc.description.statementofresponsibilityShazia Zaman, Kitamura Mitsuru, and Andrew D. Abell-
dc.language.isoen-
dc.publisherAmer Chemical Soc-
dc.source.urihttp://pubs.acs.org/cgi-bin/abstract.cgi/orlef7/2005/7/i04/abs/ol047628p.html-
dc.subjectPalladium-
dc.subjectOximes-
dc.subjectImidazoles-
dc.subjectAmino Acids-
dc.subjectCyclization-
dc.subjectCatalysis-
dc.subjectModels, Molecular-
dc.titleSynthesis of Trisubstituted Imidazoles by Palladium-Catalyzed Cyclization of O-Pentafluorobenzoylamidoximes: Application to Amino Acid Mimetics with a C-Terminal Imidazole-
dc.typeJournal article-
dc.identifier.doi10.1021/ol047628p-
pubs.publication-statusPublished-
dc.identifier.orcidAbell, A. [0000-0002-0604-2629]-
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Chemistry publications

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