Department of Chemistry

portrait of Professor Steve Ley FRS

Professor Steve Ley FRS

Trinity College

Groups: Ley group website

Telephone: 01223 336442 (fax)
             01223 336398

E-mail: svl1000@cam.ac.uk


General


In the Ley Group, we specialise in developing new synthesis methods and applying them to the construction of biologically important molecules. Over the last 4 years we have completed the total synthesis of 38 natural products including spongistatin 1 (anti-mitotic agent), rapamycin (immunosuppressant), thapsigargin (SERCA pumps inhibitor), azadirachtin (insect antifeedant) and bengazole A (fungicide), taking our group total to 140 completed total syntheses. In addition to our research on natural product synthesis, we have the Innovative Technology Centre (ITC); a new state-of-the-art flow chemistry facility. Our group is also part of the CRUK PhD Training Programme in Medicinal Chemistry.

For more detailed research information, group members and our publication list please see the group website

Publications

A mild and efficient flow procedure for the transfer hydrogenation of ketones and aldehydes using hydrous zirconia
C Battilocchio, JM Hawkins, SV Ley - Organic Letters (2013) 15, 2278
(DOI: 10.1021/ol400856g)
A Machine-Assisted Flow Synthesis of SR48692: A Probe for the Investigation of Neurotensin Receptor-1.
C Battilocchio, BJ Deadman, N Nikbin, MO Kitching, IR Baxendale, SV Ley - Chemistry (2013)
(DOI: 10.1002/chem.201300696)
The synthesis of Bcr-Abl inhibiting anticancer pharmaceutical agents imatinib, nilotinib and dasatinib.
BJ Deadman, MD Hopkin, IR Baxendale, SV Ley - Organic and Biomolecular Chemistry (2013) 11, 1766
(DOI: 10.1039/c2ob27003j)
An expeditious synthesis of imatinib and analogues utilising flow chemistry methods
MD Hopkin, IR Baxendale, SV Ley - Organic and Biomolecular Chemistry (2013) 11, 1822
(DOI: 10.1039/c2ob27002a)
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) 23, 514
(DOI: 10.1055/s-0032-1318109)
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, 1989
(DOI: 10.1039/c3sc50304f)
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, 514
Studies of a Diastereoselective Electrophilic Fluorination Reaction Employing a Cryo-Flow Reactor
K Nakayama, DL Browne, IR Baxendale, SV Ley - Synlett (2013) 24
Flow microwave technology and microreactors in synthesis
IR Baxendale, C Hornung, SV Ley, J De Mata Muñoz Molina, A Wikström - Australian Journal of Chemistry (2013) 66, 131
(DOI: 10.1071/CH12365)
Flow chemistry synthesis of zolpidem, alpidem and other GABAA agonists and their biological evaluation through the use of in-line frontal affinity chromatography
L Guetzoyan, N Nikbin, IR Baxendale, SV Ley - Chemical Science (2013) 4, 764
(DOI: 10.1039/c2sc21850j)

 

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