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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

A rapid stereocontrolled synthesis of the 3 a -hydroxy-pyrrolo[2,3- b ]indole skeleton, a building block for 10 b -hydroxy-pyrazino[1′,2′:1,5]pyrrolo[2,3- b ]indole-1,4-diones
SV Ley, E Cleator, PR Hewitt
– Org. Biomol. Chem.
(2003)
1,
3492
Reductive decomplexation of π-allyltricarbonyliron lactone complexes using sodium naphthalenide as a route to stereodefined 1,7-diols and 2,3-diene-1,7-diols
CJ Hollowood, SV Ley
– Organic and Biomolecular Chemistry
(2003)
1,
3197
Total synthesis of the phytotoxic agent herbarumin II using butane diacetals of glycolic acid as building blocks
E Diez, DJ Dixon, SV Ley, A Polara, F Rodriguez
– Synlett
(2003)
1186
A 2,3-butanedione protected chiral glycine equivalent—a new building block for the stereoselective synthesis of enantiopure N-protected α-amino acids
DJ Dixon, CI Harding, SV Ley, DMG Tilbrook
– Chemical Communications
(2003)
3,
468
Development of new synthetic tools for the preparation of biologically active molecules
SV Ley, IR Baxendale, P Grice
– CHEMICAL PROBES IN BIOLOGY: SCIENCE AT THE INTERFACE OF CHEMISTRY, BIOLOGY AND MEDICINE
(2003)
129,
235
Synthesis of enantiomers of butane-1,2-diacetal-protected glyceraldehyde and of (R,R)-butane-1,2-diacetal-protected glycolic acid
P Michel, SV Ley
– Synthesis
(2003)
1598
Fully automated multi-step solution phase synthesis using polymer supported reagents: preparation of histone deacetylase inhibitors (vol 1, pg 2419, 2003)
E Vickerstaffe, BH Warrington, M Ladlow, SV Ley
– ORGANIC & BIOMOLECULAR CHEMISTRY
(2003)
1,
2807
Transfer hydrogenation using recyclable polyurea-encapsulated palladium: efficient and chemoselective reduction of aryl ketones.
JQ Yu, HC Wu, C Ramarao, JB Spencer, SV Ley
– Chemical communications (Cambridge, England)
(2003)
678
Use of π-allyltricarbonyliron lactone complexes in the synthesis of taurospongin A: a potent inhibitor of DNA polymerase β and HIV reverse transcriptase
CJ Hollowood, S Yamanoi, SV Ley
– Org. Biomol. Chem.
(2003)
1,
1664
Supported Reagents and Scavengers in Multi-Step Organic Synthesis
IR Baxendale, SV Ley
(2003)
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Research Group

Research Interest Groups

Telephone number

01223 336398

Email address

svl1000@cam.ac.uk