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dc.contributor.authorJoyce, Jesse Jo
dc.description.abstractOrganocatalysis is a field that has bloomed over the last decades. With the field’s promise of being able to mimic nature and afford products in a synergistic manner to traditional Lewis acid catalysis, several interesting discoveries have been made. Owing to the vastness of the field as it exists today, this document will focus on two main aspects; cinchona alkaloid (and derivatives) as used in common carbon-carbon bond forming reactions and kinetic resolution via 4-dimethyl aminopyridine-N-oxide derivative driven acylation. Kinetic resolution via organocatalysis has the potential to react one enantiomer of a racemic mixture without affecting the other. The highlight of this screening was an s factor of 9 which was produced using optimized conditions using a catalyst designated DMAPO-IV. There remains much to do in improving the system and elucidating the scope of this catalytic system this report details the efforts made thus far.en_US
dc.publisherNorth Dakota State Universityen_US
dc.rightsNDSU Policy 190.6.2
dc.titleThe Development and Use of Chiral 4-Dimethylaminopyridine-N-Oxide as an Organocatalysten_US
dc.typeThesisen_US
dc.descriptionDocument incorrectly classified as a dissertation on title page (decision to classify as a thesis from NDSU Graduate School)en_US
dc.date.accessioned2019-02-06T17:37:22Z
dc.date.available2019-02-06T17:37:22Z
dc.date.issued2018en_US
dc.identifier.urihttps://hdl.handle.net/10365/29269
dc.subjectOrganocatalysis.
dc.subjectDMAPO catalysis.
dc.subjectFluxional chirality.
dc.subjectKinetic resolution.
dc.subject.lcshAcylation.en_US
dc.subject.lcshCinchona alkaloids.en_US
dc.rights.urihttps://www.ndsu.edu/fileadmin/policy/190.pdf
ndsu.degreeMaster of Science (MS)en_US
ndsu.collegeScience and Mathematicsen_US
ndsu.departmentChemistry and Biochemistryen_US
ndsu.advisorSibi, Mukund P.


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