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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 highly automated, polymer-assisted strategy for the preparation of 2-alkylthiobenzimidazoles and N,N′-dialkylbenzimidazolin-2-ones
E Vickerstaffe, BH Warrington, M Ladlow, SV Ley
– Journal of combinatorial chemistry
(2005)
7,
385
Synthesis of a Ceramide Sphingolipid as a Potential Sex Pheromone of the Hair CrabErimacrus isenbeckiiUsing Butane-2,3-diacetal Desymmetrised Glycolic Acid Building Blocks
DJ Dixon, SV Ley, S Lohmann, TD Sheppard
– Synlett
(2005)
481
The total synthesis of the annonaceous acetogenin 10-hydroxyasimicin
GL Nattrass, E Díez, MM McLachlan, DJ Dixon, SV Ley
– Angew Chem Int Ed Engl
(2005)
44,
580
Organic chemistry in ionic liquids using non-thermal energy-transfer processes
J Habermann, S Ponzi, SV Ley
– Mini-Reviews in Organic Chemistry
(2005)
2,
125
Synthesis of Alkaloid Natural Products Using Solid-Supported Reagents and Scavengers
IR Baxendale, SV Ley
– Current Organic Chemistry
(2005)
9,
1521
Total synthesis of the Fusarium toxin equisetin
LT Burke, DJ Dixon, SV Ley, F Rodríguez
– Organic and Biomolecular Chemistry
(2004)
3,
274
Organocatalysis with proline derivatives: improved catalysts for the asymmetric Mannich, nitro-Michael and aldol reactions
AJA Cobb, DM Shaw, DA Longbottom, JB Gold, SV Ley
– Org Biomol Chem
(2004)
3,
84
Preparation of enantiopure butane-2,3-diacetals of glycolic acid and alkylation reactions leading to alpha-hydroxyacid and amide derivatives
SV Ley, E Diez, DJ Dixon, RT Guy, P Michel, GL Nattrass, TD Sheppard
– Organic and Biomolecular Chemistry
(2004)
2,
3608
Studies on the generation of enolate anions from butane-2,3-diacetal protected glycolic acid derivatives and subsequent highly diastereoselective coupling reactions with aldehydes and acid chlorides.
SV Ley, DJ Dixon, RT Guy, MA Palomero, A Polara, F Rodriguez, TD Sheppard
– Organic and Biomolecular Chemistry
(2004)
2,
3618
The first Lewis acid-catalyzed allylboronate additions to aldehydes
DEA Brittain, SV Ley
– Chemtracts
(2004)
17,
620
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Research Group

Research Interest Groups

Telephone number

01223 336398

Email address

svl1000@cam.ac.uk