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
Transition Metal Catalysis in Aerobic Alcohol Oxidation Foreword
(2015)
28
VII
Development of a web-based platform for studying lithiation reactions in silico
Chemical Communications
(2015)
51
7172
(doi: 10.1039/c5cc00782h)
Foreword
(2015)
2015-January
vii
Development of a flow method for the hydroboration/oxidation of olefins.
Organic & biomolecular chemistry
(2015)
13
3871
(doi: 10.1039/c5ob00170f)
A monolith immobilised iridium Cp* catalyst for hydrogen transfer reactions under flow conditions.
Organic & Biomolecular Chemistry
(2015)
13
1768
(doi: 10.1039/c4ob02376e)
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)
Flow chemistry as a discovery tool to access sp2-sp3 cross-coupling reactions via diazo compounds.
Chem Sci
(2014)
6
1120
(doi: 10.1039/c4sc03072a)
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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