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Details of Grant 

EPSRC Reference: GR/S68095/01
Title: Cost D25 Support: Biocatalytic Asymmetric Aldol Reactions
Principal Investigator: Gouverneur, Professor V
Other Investigators:
Researcher Co-Investigators:
Project Partners:
Department: Oxford Chemistry
Organisation: University of Oxford
Scheme: Standard Research (Pre-FEC)
Starts: 20 February 2004 Ends: 19 February 2007 Value (£): 17,968
EPSRC Research Topic Classifications:
Biological & Medicinal Chem. Bioprocess Engineering
EPSRC Industrial Sector Classifications:
No relevance to Underpinning Sectors
Related Grants:
Panel History:  
Summary on Grant Application Form
While our mechanistic understanding of naturally occurring Diels-Alder is still in its infancy, more information on protein-catalysed [4+2] additions has been obtained with catalytic antibodies. Several Diels-Alderase antibodies have been generated from synthetic haptens mimicking more often the highly ordered transition state of Diels-Alder reactions. Surprisingly, only one example of antibody-mediated hetero Diels-Alder (HAD) reaction of carbonyl compounds has been reported despite the enormous synthetic potential of this particular transformation. The proposed work describes the development of a novel highly enantioselective antibody-route to access hetero Diels-Alder adducts of carbonyl compounds that we expect might be amenable to the preparation of various synthetic intermediates for natural product synthesis. A set of experiments is designed to define the scope of this novel methodology based on a tandem antibody-catalysed Mukayama-type aldol reaction followed by an intramolecular Michael addition. One of the major strand of the COSTcollaboration involves the necessary expertise of other members into mechanistic enzymology as mandatory for improved biocatalyst design, development and application.
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Organisation Website: http://www.ox.ac.uk