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

dc.contributor.author	Hunt, Ian R.	en
dc.contributor.author	Rogers, Christine	en
dc.contributor.author	Woo, Simon	en
dc.contributor.author	Rauk, Arvi	en
dc.contributor.author	Keay, Brian A.	en
dc.date.accessioned	2007-05-03T21:49:17Z
dc.date.available	2007-05-03T21:49:17Z
dc.date.issued	1995
dc.description.refereed	Yes	en
dc.identifier.citation	Hunt, 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.doi	http://dx.doi.org/10.11575/PRISM/35345
dc.identifier.issn	0002-7863
dc.identifier.uri	http://hdl.handle.net/1880/44600
dc.language.iso	eng	en
dc.publisher	American Chemical Society	en
dc.publisher.corporate	University of Calgary	en
dc.publisher.faculty	Science	en
dc.publisher.url	http://pubs.acs.org/	en
dc.subject	Chemistry	en
dc.title	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	en
dc.type	Other	en
thesis.degree.discipline	Chemistry	en