A Bicyclic L-Proline Derived Chiral Auxiliary for Asymmetric Synthesis
| Contribuinte(s) |
Department of Chemistry |
|---|---|
| Data(s) |
11/03/2016
11/03/2016
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| Resumo |
This thesis describes the use of an L−proline-derived chiral auxiliary for diastereoselective lithiation and ligand synthesis. Such compounds have been utilized in the Metallinos research group previously for the synthesis of N−substituted planar chiral ferrocenes. The first project describes the use of this chiral auxiliary as a directing group for N−benzyl substitution, providing products in up to 10:1 diastereomeric ratio (dr). These derivatives may serve as chiral ylidene precursors to serve as ligands in transition metal catalysis. In addition, an N−substituted planar chiral ferrocene ylidene ligand derived from the same chiral auxiliary was used to prepare rhodium complexes that were explored as potential catalysts for asymmetric hydroformylation. |
| Identificador | |
| Idioma(s) |
eng |
| Publicador |
Brock University |
| Palavras-Chave | #ylidene, chiral, chiral auxiliary, asymmetric, lithiation |
| Tipo |
Electronic Thesis or Dissertation |