Enantioselectivity in the Proline Catalyzed Dimerization of alpha, beta-Ionylidineacetylaldehyde, Reintal, and Related Compounds

dc.contributor.author	Wataname, Coran
dc.contributor.department	Chemistry
dc.date.accessioned	2014-01-15T20:19:27Z
dc.date.available	2014-01-15T20:19:27Z
dc.date.issued	2014-01-15
dc.description.abstract	Proteins, which play significant roles in nature, are integral parts of many biological and chemical processes. These vast macromolecules may be transport proteins, such as RBP (Retinol Binding Protein), or may bind to a substrate catalyzing a specific reaction or possibly induce an isomerization. Understanding and learning more about the chemistry involved in these protein-substrate interactions may help elucidate the mechanisms which govern them.
dc.format.extent	vi, 60 pages
dc.identifier.uri	http://hdl.handle.net/10125/32174
dc.publisher	University of Hawaii at Manoa
dc.rights	All UHM Honors Projects are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission from the copyright owner.
dc.title	Enantioselectivity in the Proline Catalyzed Dimerization of alpha, beta-Ionylidineacetylaldehyde, Reintal, and Related Compounds
dc.type	Term Project
dc.type.dcmi	Text

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