EPSRC Reference: |
GR/R51568/01 |
Title: |
A New Strategy for the use of Chiral Auxillaries in Asymmetric Synthesis |
Principal Investigator: |
Bull, Dr SD |
Other Investigators: |
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Researcher Co-Investigators: |
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Project Partners: |
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Department: |
Chemistry |
Organisation: |
University of Bath |
Scheme: |
Standard Research (Pre-FEC) |
Starts: |
01 October 2001 |
Ends: |
30 September 2004 |
Value (£): |
61,668
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EPSRC Research Topic Classifications: |
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EPSRC Industrial Sector Classifications: |
Chemicals |
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 |
This proposal describes the development of a new strategy for the use of a chiral auxiliary for the asymmetric synthesis of chiral aldehydes. The strategy employed for chiral auxiliary design relies on a stereoselective aldol reaction to generate an aldolate fragment that contains a 'temporary' stereogenic hydroxyl group. This hydroxyl group is then employed to direct areange of stereoselective reactions within the aldolate side-chain, to creat one or more new stereogenic centres. Finally, the 'temporary' hydroxyl stereogenic centre is destroyed, by virtue of a retro-aldol reaction, to regenerate the chiral auxiliary fragment and liberate the desired enantiopure aldehyde fragment. It is proposed that this approach is ideally suited to the iterative combinatorial synthesis of highly functionalised natural product fragments that contain side-chains comprosed of a series of repeating sub-units of defined stereochemistry. A strategy for the transferral of this methodology to polymer support for the combinatorial synthesis of libraries of enantiopure aldehydes is also described.
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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 |
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Project URL: |
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Further Information: |
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Organisation Website: |
http://www.bath.ac.uk |