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dc.contributorBrowne, Sheila
dc.contributorArango, Alexi
dc.contributorHamilton, Darren
dc.contributor.advisorNunez, Megan
dc.contributor.authorSchramma, Kelsey
dc.date.accessioned2012-05-07T13:37:18Z
dc.date.available2012-05-07T13:37:18Z
dc.date.issued2012-05-07
dc.identifier.urihttp://hdl.handle.net/10166/974
dc.description.abstractThis project focused on the organic chemistry reaction the vinylogous Mannich reaction. This reaction forms a carbon-carbon bond between an imine (formed from an aldehyde and amine) and a dienolate through the use of a BINOL-based catalyst. We varied the aldehyde component of this 3-component reaction by using a 1,3-diketoaldehyde. We observed that the final product was our expected cyclic tetrahydropyridine.en_US
dc.description.sponsorshipChemistryen_US
dc.language.isoen_USen_US
dc.subjectorganic chemistryen_US
dc.subjectMannich reactionen_US
dc.subjectaldehydeen_US
dc.subjectamineen_US
dc.subjectBINOL catalysten_US
dc.subjectdienolateen_US
dc.titleExamination of the Vinylogous Mannich Reaction with a 1,3-Diketoaldeydeen_US
dc.typeThesis
dc.date.gradyear2012en_US
mhc.institutionMount Holyoke College
mhc.degreeUndergraduateen_US
dc.rights.restrictedpublic


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