Exploration of new catalytic methodologies for heterocyclic synthesis and C-C Bond Formation.
Amino boronate based bifiinctional molecules have the potential to be powerful catalysts. Herein, a number of approaches to the bifimctional benzimidazole catalyst 1 are described, and the synthesis of a number of analogues are explored. Investigations into the potential of 2-(2-boronobenzene)- 2N-n-butylbenzimidazole sodium hydroxide salt 1 as a catalyst for a number of synthetic transformations, including an aza-version of the Baeyer-Villiger reaction (Equation 1), are described The 2-(2-boronobenzene)-N-n-butylbenzimidazole sodium hydroxide salt 1 is shown to be active in the aldol condensation reaction (Equation 2), Knoevenagel reaction, and evidence for the promotion of the Michael reaction by 1 is presented. The mechanism by which the aldol condensation reaction is promoted by 1 is explored through kinetic studies.
| Item Type | Thesis (Unspecified) |
|---|---|
| Divisions | Faculty of Science > Chemistry, Department of |
| Historic department | Chemistry |
| Date Deposited | 09 Sep 2011 08:54 |
| Last Modified | 30 Mar 2026 19:40 |
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picture_as_pdf - 2795_873.pdf
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folder_zip - Blatch_Thesis.zip
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subject - Supplemental Material
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subject - X-ray diffraction data for compound 52, 61, 65, 106, 137