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
Continuous-Flow Processing of Gaseous Ammonia Using a Teflon AF-2400 Tube-in-Tube Reactor: Synthesis of Thioureas and In-Line Titrations
Synlett
(2012)
23
1402
(doi: 10.1055/s-0031-1290963)
A Flow-Based Synthesis of 2-Aminoadamantane-2-carboxylic Acid
Organic Process Research & Development
(2012)
16
798
(doi: 10.1021/op300084z)
Flow synthesis using gaseous ammonia in a Teflon AF-2400 tube-in-tube reactor: Paal-Knorr pyrrole formation and gas concentration measurement by inline flow titration.
Organic and Biomolecular Chemistry
(2012)
10
5774
(doi: 10.1039/c2ob25407g)
Discovery, design and synthesis of a novel series of non-peptidomimetic inhibitors of XIAP-caspase 9 interactions
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2012)
243
The Lab of the Future. the importance of remote monitoring and control
Chimica Oggi Chemistry Today
(2012)
30
24
Increased endothelial cell selectivity of triazole-bridged dihalogenated A-ring analogues of combretastatin A-1
Bioorganic and Medicinal Chemistry
(2012)
20
1749
(doi: 10.1016/j.bmc.2012.01.010)
The molecular basis for selective inhibition of unconventional mRNA splicing by an IRE1-binding small molecule.
Proc Natl Acad Sci U S A
(2012)
109
e869
(doi: 10.1073/pnas.1115623109)
Scale-up of flow-assisted synthesis of C 2-symmetric chiral PyBox ligands
Synthesis
(2012)
44
635
(doi: 10.1055/s-0031-1289676)
A-ring dihalogenation increases the cellular activity of combretastatin-templated tetrazoles
ACS Medicinal Chemistry Letters
(2012)
3
177
(doi: 10.1021/ml200149g)
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