Examination of the Vinylogous Mannich Reaction with a 1,3-Diketoaldeyde
| dc.contributor | Browne, Sheila | |
| dc.contributor | Arango, Alexi | |
| dc.contributor | Hamilton, Darren | |
| dc.contributor.advisor | Nunez, Megan | |
| dc.contributor.author | Schramma, Kelsey | |
| dc.date.accessioned | 2012-05-07T13:37:18Z | |
| dc.date.available | 2012-05-07T13:37:18Z | |
| dc.date.gradyear | 2012 | en_US |
| dc.date.issued | 2012-05-07 | |
| dc.description.abstract | This 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.sponsorship | Chemistry | en_US |
| dc.identifier.uri | http://hdl.handle.net/10166/974 | |
| dc.language.iso | en_US | en_US |
| dc.rights.restricted | public | |
| dc.subject | organic chemistry | en_US |
| dc.subject | Mannich reaction | en_US |
| dc.subject | aldehyde | en_US |
| dc.subject | amine | en_US |
| dc.subject | BINOL catalyst | en_US |
| dc.subject | dienolate | en_US |
| dc.title | Examination of the Vinylogous Mannich Reaction with a 1,3-Diketoaldeyde | en_US |
| dc.type | Thesis | |
| mhc.degree | Undergraduate | en_US |
| mhc.institution | Mount Holyoke College |