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Yusuf Hamied Department of Chemistry

 

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 last 10 years we have completed the total synthesis of 28 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 150 completed total syntheses. In addition to our research on natural product synthesis, we also have a new state-of-the-art flow chemistry facility. 

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

Publications

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
A prototype device for evaporation in batch and flow chemical processes
BJ Deadman, C Battilocchio, E Sliwinski, SV Ley
– Green Chemistry
(2013)
15,
2050
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
– Chemical Science
(2013)
4,
764
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,
159
An expeditious synthesis of imatinib and analogues utilising flow chemistry methods.
MD Hopkin, IR Baxendale, SV Ley
– Organic and Biomolecular Chemistry
(2012)
11,
1822
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
(2012)
11,
1766
Synthesis and use of a trifluoromethylated azomethine ylide precursor.
G Tran, R Meier, L Harris, DL Browne, SV Ley
– The Journal of Organic Chemistry
(2012)
77,
11071
Flow Microwave Technology and Microreactors in Synthesis
IR Baxendale, C Hornung, SV Ley, J De Mata Muñoz Molina, A Wikström
– Australian Journal of Chemistry
(2012)
66,
131
Synthesis of Enantiomerically Enriched 3-Amino-2-oxindoles through a Palladium-Mediated Asymmetric Intramolecular Arylation of α-Ketimino Amides
P Tolstoy, SXY Lee, C Sparr, SV Ley
– Org Lett
(2012)
14,
4810
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Research Group

Research Interest Groups

Telephone number

01223 336398

Email address

svl1000@cam.ac.uk