Why Do Catalytic Quantities of Lewis Acid Generally Yield More Product than 1.1 Equivalent in the Intramolecular Diels-Alder Reaction with a Furan Diene? Competitive Complexation NMR Studies Provide an Answer

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dc.contributor.authorHunt, Ian R.en
dc.contributor.authorRogers, Christineen
dc.contributor.authorWoo, Simonen
dc.contributor.authorRauk, Arvien
dc.contributor.authorKeay, Brian A.en
dc.date.accessioned2007-05-03T21:49:17Z
dc.date.available2007-05-03T21:49:17Z
dc.date.issued1995
dc.description.refereedYesen
dc.identifier.citationHunt, I.R., Rogers, C., Woo, S., Rauk, A. and Keay, B.A.. (1995). "Why Do Catalytic Quantities of Lewis Acid Generally Yield More Product than 1.1 Equivalent in the Intramolecular Diels-Alder Reaction with a Furan Diene? Competitive Complexation NMR Studies Provide an Answer". Journal of American Chemical Society, 117, No. 3: 1049-1056.en
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/35345
dc.identifier.issn0002-7863
dc.identifier.urihttp://hdl.handle.net/1880/44600
dc.language.isoengen
dc.publisherAmerican Chemical Societyen
dc.publisher.corporateUniversity of Calgaryen
dc.publisher.facultyScienceen
dc.publisher.urlhttp://pubs.acs.org/en
dc.subjectChemistryen
dc.titleWhy Do Catalytic Quantities of Lewis Acid Generally Yield More Product than 1.1 Equivalent in the Intramolecular Diels-Alder Reaction with a Furan Diene? Competitive Complexation NMR Studies Provide an Answeren
dc.typeOtheren
thesis.degree.disciplineChemistryen
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