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

Microwave‐Assisted Suzuki Coupling Reactions with an Encapsulated Palladium Catalyst for Batch and Continuous‐Flow Transformations
IR Baxendale, CM Griffiths-Jones, SV Ley, GK Tranmer
Chemistry - A European Journal
(2006)
12
The use of polymer-supported reagents and scavengers in the synthesis of natural products
SV Ley, IR Baxendale, RM Myers
(2006)
Effect of azadirachtin‐derived decalin (perhydronaphthalene) and dihydrofuranacetal (furo[2, 3‐fo]pyran) fragments on the feeding behaviour of Spodoptera littoralis
WM Blaney, MSJ Simmonds, SV Ley, JC Anderson, SC Smith, A Wood
Pesticide Science
(2006)
40
Microwave flow chemistry: the next evolutionary step in synthetic chemistry?
IR Baxendale, MR Pitts
Chimica Oggi
(2006)
24
Progress towards avermectins and milbemycins
SV Ley
Pest Management Science
(2006)
18
Targeting C-reactive protein for the treatment of cardiovascular disease.
MB Pepys, GM Hirschfield, GA Tennent, JR Gallimore, MC Kahan, V Bellotti, PN Hawkins, RM Myers, MD Smith, A Polara, AJA Cobb, SV Ley, JA Aquilina, CV Robinson, I Sharif, GA Gray, CA Sabin, MC Jenvey, SE Kolstoe, D Thompson, SP Wood
Nature
(2006)
440
Chemical variation of natural product-like scaffolds: design and synthesis of spiroketal derivatives
G Zinzalla, L-G Milroy, SV Ley
Organic & Biomolecular Chemistry
(2006)
4
An efficient, asymmetric organocatalyst-mediated conjugate addition of nitroalkanes to unsaturated cyclic and acyclic ketones.
CET Mitchell, SE Brenner, J García-Fortanet, SV Ley
Org Biomol Chem
(2006)
4
A highly enantioselective total synthesis of (+)- goniodiol
EW Tate, DJ Dixon, SV Ley
Organic & Biomolecular Chemistry
(2006)
4
A flow process for the multi-step synthesis of the alkaloid natural product oxomaritidine: a new paradigm for molecular assembly
IR Baxendale, J Deeley, CM Griffiths-Jones, SV Ley, S Saaby, GK Tranmer
Chem Commun (Camb)
(2006)

Research Group

Telephone number

01223 336398

Email address