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 syntheses of natural products containing spirocarbocycles
Org Biomol Chem
(2015)
13
9907
(doi: 10.1039/c5ob01524c)
Development of a web-based platform for studying lithiation reactions in silico
Chemical communications (Cambridge, England)
(2015)
51
7172
(doi: 10.1039/c5cc00782h)
Development of a flow method for the hydroboration/oxidation of olefins.
Organic & biomolecular chemistry
(2015)
13
3871
(doi: 10.1039/c5ob00170f)
Cyclopropanation using flow-generated diazo compounds.
Org Biomol Chem
(2015)
13
2550
(doi: 10.1039/c5ob00019j)
Achieving Continuous Manufacturing: Technologies and Approaches for Synthesis, Workup, and Isolation of Drug Substance May 20–21, 2014 Continuous Manufacturing Symposium
Journal of pharmaceutical sciences
(2014)
104
781
(doi: 10.1002/jps.24252)
Total syntheses of linear polythiazole/oxazole plantazolicin A and its biosynthetic precursor plantazolicin B
Angewandte Chemie (International ed. in English)
(2014)
54
1284
(doi: 10.1002/anie.201410063)
Sustainable synthesis of thioimidazoles via carbohydrate-based multicomponent reactions
Organic letters
(2014)
16
6076
(doi: 10.1021/ol502845h)
A Systems Approach towards an Intelligent and Self‐Controlling Platform for Integrated Continuous Reaction Sequences
Angewandte Chemie (International ed. in English)
(2014)
54
144
(doi: 10.1002/anie.201409356)
Facilitating Biomimetic Syntheses of Borrerine Derived Alkaloids by Means of Flow-Chemical Methods*
Australian Journal of Chemistry
(2014)
68
693
(doi: 10.1071/ch14530)
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