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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

Use of the Temporary Connection in Organic Synthesis
LR Cox, SV Ley
(2007)
274
A new asymmetric organocatalytic nitrocyclopropanation reaction
HM Hansen, DA Longbottom, SV Ley
– Chemical communications (Cambridge, England)
(2006)
4838
A flow reactor process for the synthesis of peptides utilizing immobilized reagents, scavengers and catch and release protocols.
IR Baxendale, SV Ley, CD Smith, GK Tranmer
– Chemical Communications
(2006)
4835
Sulphuration of Electron-Rich Arenes with Sulphenamides and Aminosulphenyl Chlorides
MU BOMBALA, SV LEY
– Synthetic Communications
(2006)
10,
291
Polymer-supported reagents and scavengers in synthesis
SV Ley, IR Baxendale, RM Myers
(2006)
3,
791
Fully Automated Continuous Flow Synthesis of 4,5-Disubstituted Oxazoles
M Baumann, IR Baxendale, SV Ley, CD Smith, GK Tranmer
– Organic letters
(2006)
8,
5231
Stereocontrolled Total Synthesis of Bengazole A: A Marine Bisoxazole Natural Product Displaying Potent Antifungal Properties
JA Bull, EP Balskus, RAJ Horan, M Langner, SV Ley
– Angewandte Chemie International Edition
(2006)
45,
6714
An enantioselective organocatalytic route to chiral 3,6-dihydropyridazines from aldehydes
AJ Oelke, S Kumarn, DA Longbottom, SV Ley
– Synlett
(2006)
2006,
2548
ORGN 141-Asymmetric organocatalytic conjugate addition of malonates to enones using a proline tetrazole catalyst
KR Knudsen, CET Mitchell, S Brenner, SV Ley
– ABSTR PAP AM CHEM S
(2006)
232,
Enantioselective catalytic intramolecular cyclopropanation using modified cinchona alkaloid organocatalysts
CCC Johansson, N Bremeyer, SV Ley, DR Owen, SC Smith, MJ Gaunt
– Angewandte Chemie (International ed. in English)
(2006)
45,
6024
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Research Group

Research Interest Groups

Telephone number

01223 336398

Email address

svl1000@cam.ac.uk