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
Engineering chemistry: integrating batch and flow reactions on a single, automated reactor platform
Reaction Chemistry & Engineering
(2016)
1
629
(doi: 10.1039/c6re00160b)
Visible Light Activation of Boronic Esters Enables Efficient Photoredox C(sp$^2$)-C(sp$^3$) Cross-Couplings in Flow
Angewandte Chemie (International ed. in English)
(2016)
128
14085
(doi: 10.1002/anie.201605548)
Combination of Enabling Technologies to Improve and Describe the Stereoselectivity of Wolff-Staudinger Cascade Reaction
Synthesis
(2016)
48
3515
(doi: 10.1055/s-0035-1562579)
Promiscuous targeting of bromodomains by bromosporine identifies BET proteins as master regulators of primary transcription response in leukemia
Science Advances
(2016)
2
e1600760
(doi: 10.1126/sciadv.1600760)
Continuous Processing and Efficient $\textit{in Situ}$ Reaction Monitoring of a Hypervalent Iodine(III) Mediated Cyclopropanation Using Benchtop NMR Spectroscopy
Organic Process Research & Development
(2016)
20
1603
(doi: 10.1021/acs.oprd.6b00177)
The Total Synthesis of the Bioactive Natural Product Plantazolicin A and Its Biosynthetic Precursor Plantazolicin B.
Chemistry
(2016)
22
15902
(doi: 10.1002/chem.201603157)
Flow enabled peptide synthesis
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2016)
252
Taming hazardous chemistry by continuous flow technology
Chemical Society reviews
(2016)
45
4892
(doi: 10.1039/c5cs00902b)
A multicomponent approach for the preparation of homoallylic alcohols.
Chem Sci
(2016)
7
6803
(doi: 10.1039/c6sc02581a)
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