Show simple item record

dc.contributor.advisorMattson, Anita
dc.creatorGarza, Victoria
dc.date.accessioned2012-05-28T01:40:08Z
dc.date.available2012-05-28T01:40:08Z
dc.date.issued2012-06
dc.identifier.urihttp://hdl.handle.net/1811/51891
dc.description.abstractReactions catalyzed by small organic molecules through non-covalent interactions are emerging as powerful tools for the synthesis of valuable target molecules. Specifically, hydrogen bond donors (HBDs) are useful non-covalent catalysts able to interact with a variety of functional groups and operate in a number of transformations. Boronate ureas have been identified as a new class of HBDs with enhanced reactivity due to the strategic placement of an internal Lewis acid. Specifically, in comparison to conventional ureas, boronate ureas benefit from lower catalyst loadings, reduced reaction times and access to unique reactivity patterns. To this end, we have discovered boronate ureas operate as catalysts for the ring-opening of strained ring systems, giving rise to valuable building blocks in good yield.en_US
dc.language.isoen_USen_US
dc.publisherThe Ohio State Universityen_US
dc.relation.ispartofseriesThe Ohio State University. Department of Chemistry Honors Theses; 2012en_US
dc.subjectchemistryen_US
dc.subjectcatalysisen_US
dc.subjectstrained ringsen_US
dc.subjectboronate ureaen_US
dc.titleBoronate Urea Activation of Strained Ringsen_US
dc.typeThesisen_US
dc.description.embargoNo embargoen_US


Files in this item

Thumbnail

Items in Knowledge Bank are protected by copyright, with all rights reserved, unless otherwise indicated.

This item appears in the following Collection(s)

Show simple item record