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New Dearomatization Methods for Chemical Synthesis and Synthetic Biology

Objective

The hypothesis behind our synthesis blueprint involves the development of new dearomatization process that comprises phenol oxidative dearomatization and organocatalytic desymmetrization, generating highly functionalized, non-racemic architectures. A key aspect of this process is the formation of quaternary centres embedded within a complex structural framework containing valuable orthogonal functionality. With this in mind, we have identified classes of molecules that could be accessed through exploitation and developments of this methodology. The natural product targets encompass structures of alkaloids such as morphine, as well as complex non-natural frameworks that may have interesting properties as the basis for novel small-molecule libraries. Also we have identified that dearomatization could be a useful tool in synthetic biology wherein tyrosine residues are targets for selective oxidation and conjugated with a suitable reagent of function. This will lead to an exciting new tool for chemical biology. The overall proposal is split into three objective research plans comprising (i) the development of CED methodology (ii) the synthesis of morphine, and (iii) the development of deraromatization methods for synthetic biology.

Call for proposal

FP7-PEOPLE-2012-IIF
See other projects for this call

Coordinator

THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
EU contribution
€ 221 606,40
Address
TRINITY LANE THE OLD SCHOOLS
CB2 1TN Cambridge
United Kingdom

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Region
East of England East Anglia Cambridgeshire CC
Activity type
Higher or Secondary Education Establishments
Administrative Contact
Renata Schaeffer (Ms.)
Links
Total cost
No data