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
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic and Biomolecular Chemistry
(2005)
3
4095
(doi: 10.1039/b512410g)
Evolution or Revolution: The Challenge to the Modern Medicinal Chemist
(2005)
1
Total synthesis of two novel subpicomolar sarco/endoplasmatic reticulum Ca2+-ATPase inhibitors designed by an analysis of the binding site of thapsigargin.
Journal of medicinal chemistry
(2005)
48
7005
(doi: 10.1021/jm058036v)
Synthesis of Alkaloid Natural Products Using Solid-Supported Reagents and Scavengers
Current Organic Chemistry
(2005)
9
1521
(doi: 10.2174/138527205774370513)
A versatile organocatalyst for the asymmetric conjugate addition of nitroalkanes to enones
Chem Commun (Camb)
(2005)
5346
(doi: 10.1039/b511441a)
A highly selective, organocatalytic route to chiral dihydro-1,2-oxazines
Organic letters
(2005)
7
4189
(doi: 10.1021/ol051577u)
Total Synthesis of Spongistatin 1: A Synthetic Strategy Exploiting Its Latent Pseudo‐Symmetry
Angewandte Chemie (International ed. in English)
(2005)
44
5433
(doi: 10.1002/anie.200502008)
Non-metal-catalysed intramolecular alkyne cyclotrimerization reactions promoted by focussed microwave heating in batch and flow modes.
Organic & biomolecular chemistry
(2005)
3
3365
(doi: 10.1039/b509540a)
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