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

Continuous Cold without Cryogenic Consumables: Development of a Convenient Laboratory Tool for Low‐Temperature Flow Processes
DL Browne, BH Harji, SV Ley
Chemical Engineering & Technology
(2013)
36
Synthesis of spongistatin 2 employing a new route to the EF fragment
H Kraus, A Français, M O'Brien, J Frost, A Diéguez-Vázquez, A Polara, N Baricordi, R Horan, D-S Hsu, T Tsunoda, SV Ley
Chemical Science
(2013)
4
The integration of flow reactors into synthetic organic chemistry
IR Baxendale
Journal of Chemical Technology and Biotechnology
(2013)
88
Synthesis of (-)-hennoxazole A: Integrating batch and flow chemistry methods
A Fernández, ZG Levine, M Baumann, S Sulzer-Mossé, C Sparr, S Schläger, A Metzger, IR Baxendale, SV Ley
Synlett
(2013)
24
Flow chemistry synthesis of zolpidem, alpidem and other GABA A agonists and their biological evaluation through the use of in-line frontal affinity chromatography
L Guetzoyan, N Nikbin, IR Baxendale, SV Ley
Chem. Sci.
(2013)
4
A prototype device for evaporation in batch and flow chemical processes
BJ Deadman, C Battilocchio, E Sliwinski, SV Ley
Green Chemistry
(2013)
15
A Continuous Flow Solution to Achieving Efficient Aerobic Anti-Markovnikov Wacker Oxidation
SL Bourne, SV Ley
Advanced Synthesis and Catalysis
(2013)
342
Flow Chemistry Syntheses of Styrenes, Unsymmetrical Stilbenes and Branched Aldehydes
SL Bourne, M O'Brien, S Kasinathan, P Koos, P Tolstoy, DX Hu, RW Bates, B Martin, B Schenkel, SV Ley
Chemcatchem
(2012)
5
An expeditious synthesis of imatinib and analogues utilising flow chemistry methods.
MD Hopkin, IR Baxendale, SV Ley
Organic & biomolecular chemistry
(2012)
11
The synthesis of Bcr-Abl inhibiting anticancer pharmaceutical agents imatinib, nilotinib and dasatinib
BJ Deadman, MD Hopkin, IR Baxendale, SV Ley
Org Biomol Chem
(2012)
11

Research Group

Telephone number

01223 336398

Email address