Director of Research
In the Ley Group, we specialise in developing new synthesis methods and applying them to the construction of biologically important molecules. Over the years we have completed the total synthesis of many natural products, including: spongistatin 1 (anti-mitotic agent); rapamycin (immunosuppressant); thapsigargin (SERCA pumps inhibitor); azadirachtin (insect antifeedant); and bengazole A (fungicide). In addition to our research on natural product synthesis, we also pioneered flow chemistry and machine assisted synthesis.
For more detailed research information and our publication list, please see our legacy group website.
Completed Natural Products

Publications
Total synthesis studies on macrocyclic pipecolic acid natural products: FK506, the antascomicins and rapamycin
Progress in Drug Research
(2008)
66
13
(doi: 10.1007/978-3-7643-8595-8_2)
Microreactors in organic synthesis and catalysis
(2008)
PtCl4-catalyzed domino synthesis of fused bicyclic acetals
Angew Chem Int Ed Engl
(2007)
47
209
(doi: 10.1002/anie.200704595)
Microwave reactions under continuous flow conditions
Comb Chem High Throughput Screen
(2007)
10
802
(doi: 10.2174/138620707783220374)
A flow process for the multistep synthesis of the alkaloid natural product oxomaritidine: A new paradigm for molecular assembly
Chemtracts
(2007)
20
462
The development and application of supported reagents for multi-step organic synthesis
SUPPORTED CATALYSTS AND THEIR APPLICATIONS
(2007)
9
(doi: 10.1039/9781847551962-00009)
[MR-based tridirectional flow imaging. Acquisition and 3D analysis of flows in the thoracic aorta].
Die Radiologie
(2007)
47
1012
(doi: 10.1007/s00117-007-1577-6)
A relay route for the synthesis of azadirachtin
Angew Chem Int Ed Engl
(2007)
46
7633
(doi: 10.1002/anie.200703028)
Synthesis of Azadirachtin: A Long but Successful Journey
Angew Chem Int Ed Engl
(2007)
46
7629
(doi: 10.1002/anie.200703027)
Synthesis of antifeedants for insects: novel behaviour-modifying chemicals from plants.
Ciba Foundation symposium
(2007)
154
80
(doi: 10.1002/9780470514009.ch7)
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