EPSRC Reference: |
GR/M94922/02 |
Title: |
DEVELOPING A USEFUL DIELS-ALDER METHODOLOGY WITH DIFLUORINATED DIENOPHILES |
Principal Investigator: |
Percy, Professor JM |
Other Investigators: |
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Researcher Co-Investigators: |
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Project Partners: |
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Department: |
Chemistry |
Organisation: |
University of Leicester |
Scheme: |
Standard Research (Pre-FEC) |
Starts: |
01 September 2001 |
Ends: |
29 February 2004 |
Value (£): |
92,016
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EPSRC Research Topic Classifications: |
Chemical Synthetic Methodology |
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EPSRC Industrial Sector Classifications: |
Chemicals |
Pharmaceuticals and Biotechnology |
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Related Grants: |
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Panel History: |
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Summary on Grant Application Form |
Metallate difluoroenol carbamate chemistry has enabled us to synthesise dienophiles which contain two fluorine atoms. We are therefore now able to synthesise highly-functionalised six-membered carbocycles that contain two fluorine atoms using the Diels-Alder reaction. In this project, we wish to optimise the synthesis of our dienophiles by replacing the potentially hazardous organotin chemistry, and perform cycloadditions with a wide range of dienes under Lewis acid-catlysed conditions, learning about the nature of Lewis acid binding along the way. Key elements of functional group chemistry will then be addressed culminating in illustrative racemic syntheses of analogues of cyclitol natural products (Streptol, Zeylenol, Validamine, Valienamine). Importantly, the programme will provide underpinning technology for researchers in areas where fluorine atom incorporation has yielded novel applications compounds, such as medicine (pharmaceuticals) and agrochemicals.
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Key Findings |
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Potential use in non-academic contexts |
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Impacts |
Description |
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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.le.ac.uk |