EPSRC Reference: |
GR/R96835/01 |
Title: |
Concise Syntheses of Fluoroanalogues of Cyclitols and Sugars |
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 April 2003 |
Ends: |
31 March 2006 |
Value (£): |
277,108
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EPSRC Research Topic Classifications: |
Chemical Synthetic Methodology |
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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 |
Allyl ethers of trifluoroethanol undergo dehydrofluorination/metallation to afford difluoroalkenylmetals which can be trapped with alpha, beta-unsatu rate aldehydes to afford difluorinated dienols. A tandem process involving Claisen rearrangement followed by reduction, affords highly-functionalised 1,7octadienes which can be converted to mono- or difluorinated cyclohexenes via ring-closing metathesis (RCM). The proposed sequences offer high levels of stereocontrol and the prospect of the availability of diverse arrays of novel cyclitol and monosaccharide analogues. The sequences are shor minimise the use of protecting group chemistry and use readily-available and inexpensive starting materials. The products include analogues of monosaccharides, and of cyclitols or carbasugars.
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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.le.ac.uk |