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
Pinene-derived bipyridine ligands (PINDY) in asymmetric catalysis.
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2000)
219
U132
Asymmetric molybdenum-catalyzed allylic substitution.
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2000)
219
U132
Polymer supported reagents in synthesis: Preparation of bicyclo[2.2.2]octane derivatives via tandem Michael addition reactions and subsequent combinatorial decoration
Journal of combinatorial chemistry
(2000)
2
104
(doi: 10.1021/cc9900697)
Rapid assembly of oligosaccharides: 1,2-diacetal-mediated reactivity tuning in the coupling of glycosyl fluorides
Tetrahedron Asymmetry
(2000)
11
173
A Short and Efficient Stereoselective Synthesis of the Polyhydroxylated Macrolactone (+)-Aspicilin
Org Lett
(2000)
2
123
(doi: 10.1021/ol991214s)
Reductive decomplexation of π-allyltricarbonyliron lactone complexes:: a new route to stereodefined acyclic 1,5-diols and 1,5,7-triols
Journal of the Chemical Society, Perkin Transactions 1
(2000)
211
(doi: 10.1039/a907630a)
Clean and efficient synthesis of azo dyes using polymer-supported reagents
Green Chemistry
(2000)
2
43
(doi: 10.1039/b000816h)
A Short and Efficient Stereoselective Synthesis of the Potent 5-Lipoxygenase Inhibitor CMI-977
Synthetic Communications
(2000)
30
1955
(doi: 10.1080/00397910008087245)
Parallel solution-phase syntheses of functionalised bicyclo[2.2.2]octanes: generation of a library using orchestrated multi-step sequences of polymer-supported reagents and sequesterants
Journal of the Chemical Society Perkin Transactions 1
(2000)
3645
(doi: 10.1039/b003129l)
New strategies for organic catalysis: The first highly enantioselective organocatalytic Diels-Alder reaction
Chemtracts
(2000)
13
592
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