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

Welcome to Reaction Chemistry & Engineering
SA Khan, IR Baxendale, JM Hawkins, SV Ley, K Jensen, V Hessel, G Luo, D Blackmond, A Katz, DG Vlachos, ME Davis
Reaction Chemistry & Engineering
(2016)
1
Flow enabled peptide synthesis
Z Wilson, S Ley
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2016)
252
Continuous-Flow Synthesis of 2H-Azirines and Their Diastereoselective Transformation to Aziridines
M Baumann, I Baxendale
Synlett
(2015)
27
Controlled Flow Precipitation as a Valuable Tool for Synthesis
P Filipponi, A Gioiello, IR Baxendale
Organic Process Research & Development
(2015)
20
Synthesis of 1,3,6-Trisubstituted Azulenes
TO Leino, M Baumann, J Yli-Kauhaluoma, IR Baxendale, EAA Wallén
The Journal of organic chemistry
(2015)
80
A Novel Internet-Based Reaction Monitoring, Control and Autonomous Self-Optimization Platform for Chemical Synthesis
DE Fitzpatrick, C Battilocchio, SV Ley
Organic Process Research & Development
(2015)
20
Synthesis of a Precursor to Sacubitril Using Enabling Technologies.
S-H Lau, SL Bourne, B Martin, B Schenkel, G Penn, SV Ley
Org Lett
(2015)
17
Batch and Flow Synthesis of Pyrrolo[1,2-a]-quinolines via an Allene-Based Reaction Cascade
M Baumann, IR Baxendale
The Journal of organic chemistry
(2015)
80
Corrigendum to “Design, synthesis and evaluation of semi-synthetic triazole-containing caffeic acid analogues as 5-lipoxygenase inhibitors” [Eur. J. Med. Chem. 101 (2015) 573–583]
D de Lucia, OM Lucio, B Musio, A Bender, M Listing, S Dennhardt, A Koeberle, U Garscha, R Rizzo, S Manfredini, O Werz, SV Ley
European Journal of Medicinal Chemistry
(2015)
103
Modeling mesoscale reactors for the production of fine chemicals
PM Witt, S Somasi, I Khan, DW Blaylock, JA Newby, SV Ley
Chemical Engineering Journal
(2015)
278

Research Group

Telephone number

01223 336398

Email address