EPSRC Reference: |
GR/R86744/01 |
Title: |
New Hydroxamic Acid Ligands for Asymmetric catalysis |
Principal Investigator: |
Malkov, Professor A |
Other Investigators: |
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Researcher Co-Investigators: |
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Project Partners: |
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Department: |
School of Chemistry |
Organisation: |
University of Glasgow |
Scheme: |
Fast Stream |
Starts: |
01 October 2002 |
Ends: |
30 September 2005 |
Value (£): |
63,066
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EPSRC Research Topic Classifications: |
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EPSRC Industrial Sector Classifications: |
Chemicals |
Pharmaceuticals and Biotechnology |
No relevance to Underpinning Sectors |
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Related Grants: |
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Panel History: |
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Summary on Grant Application Form |
New efficient chiral ligands with the hydroxamic acid core will be designed for vanadium catalysed asymmetric epoxidation and related Lewis acid catalysed reactions. The purpose of this project is to overcome the notorious in vanadium epoxidation catalysis ligand deceleration effect and improve enantioselectivity. The research will be inspired by our preliminary results which show substantial acceleration and modest to good enantioselectivity. The role of various structural features on the effectiveness of the reaction will be studied. The accelerating effect of an additional functional group in the ligand on the reactivity, combined with the effect of chirality relay by substituted amide observed for related systems, should lead to the development of new very effective catalytic epoxidation systems based on vanadium complexes.
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Key Findings |
This information can now be found on Gateway to Research (GtR) http://gtr.rcuk.ac.uk
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Potential use in non-academic contexts |
This information can now be found on Gateway to Research (GtR) http://gtr.rcuk.ac.uk
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Impacts |
Description |
This information can now be found on Gateway to Research (GtR) http://gtr.rcuk.ac.uk |
Summary |
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Date Materialised |
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Sectors submitted by the Researcher |
This information can now be found on Gateway to Research (GtR) http://gtr.rcuk.ac.uk
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Project URL: |
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Further Information: |
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Organisation Website: |
http://www.gla.ac.uk |