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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

Sequence-based Process Modeling of Fluidized Bed Biomass Gasification
C Schotten, D Plaza, S Manzini, SP Nolan, SV Ley, DL Browne, A Lapkin
– ACS Sustainable Chemistry & Engineering
(2015)
3,
2640
A Short Multistep Flow Synthesis of a Potential Spirocyclic Fragrance Component
IR Baxendale
– Chemical Engineering & Technology
(2015)
38,
1713
The Use of Gases in Flow Synthesis
CJ Mallia, IR Baxendale
– Organic Process Research & Development
(2015)
20,
327
Foreword
SV Ley
(2015)
xiii
Callipeltosides A, B and C: Total Syntheses and Structural Confirmation.
JR Frost, CM Pearson, TN Snaddon, RA Booth, RM Turner, J Gold, DM Shaw, MJ Gaunt, SV Ley
– Chemistry – A European Journal
(2015)
21,
13261
The synthesis of active pharmaceutical ingredients (APIs) using continuous flow chemistry.
M Baumann, IR Baxendale
– Beilstein J Org Chem
(2015)
11,
1194
Machine‐Assisted Organic Synthesis
SV Ley, DE Fitzpatrick, RM Myers, C Battilocchio, RJ Ingham
– Angewandte Chemie International Edition
(2015)
54,
10122
Design, synthesis and evaluation of semi-synthetic triazole-containing caffeic acid analogues as 5-lipoxygenase inhibitors
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,
573
Generation of Reactive Ketenes under Flow Conditions through Zinc-Mediated Dehalogenation
A Hafner, SV Ley
– Synlett
(2015)
26,
1470
Machines vs Malaria: A Flow-Based Preparation of the Drug Candidate OZ439
S-H Lau, A Galván, RR Merchant, C Battilocchio, JA Souto, MB Berry, SV Ley
– Org Lett
(2015)
17,
3218
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Research Group

Research Interest Groups

Telephone number

01223 336398

Email address

svl1000@cam.ac.uk