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
Polymer supported reagents in synthesis: Preparation of bicyclo[2.2.2]octane derivatives via tandem Michael addition reactions and subsequent combinatorial decoration
ACS Combinatorial Science
(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
Organic letters
(2000)
2
123
(doi: 10.1021/ol991214s)
New strategies for organic catalysis: The first highly enantioselective organocatalytic Diels-Alder reaction
Chemtracts
(2000)
13
592
Tri-n-butyl[2-(trimethylsilyl)-ethoxymethoxymethyl]stannane: A convenient hydroxymethyl anion equivalent
Synlett
(2000)
2000
455
(doi: 10.1055/s-2000-6559)
Deracemization of Baylis-Hillman adducts
Chemtracts
(2000)
13
596
Preparation of desymmetrized meso-tartrate derivatives: Synthesis and utility of (R′,R′,R,-S)-2,3-butane diacetal protected dimethyl tartrate
Chemtracts
(2000)
13
66
Asymmetric molybdenum-catalyzed allylic substitution.
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2000)
219
U132
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)
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CHEMISTRY IN BRITAIN
(2000)
36
23
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