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 years we have completed the total synthesis of many natural products, including: spongistatin 1 (anti-mitotic agent); rapamycin (immunosuppressant); thapsigargin (SERCA pumps inhibitor); azadirachtin (insect antifeedant); and bengazole A (fungicide). In addition to our research on natural product synthesis, we also pioneered flow chemistry and machine assisted synthesis. 

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

Completed Natural Products

Publications

Polymer-supported hypervalent iodine reagents in 'clean' organic synthesis with potential application in combinatorial chemistry
SV Ley, AW Thomas, H Finch
Journal of the Chemical Society Perkin Transactions 1
(1999)
Molybdenum(II)- and Tungsten(II)-Catalyzed Allylic Substitution.
AV Malkov, IR Baxendale, D Dvorák, DJ Mansfield, P Kocovský
The Journal of Organic Chemistry
(1999)
64
Molybdenum(II)-catalyzed allylation of electron-rich aromatics and heteroaromatics
AV Malkov, SL Davis, IR Baxendale, WL Mitchell, P Kocovský
The Journal of Organic Chemistry
(1999)
64
1,7-Induction of chirality in Mukaiyama aldol reactions using π- allyltricarbonyliron lactone and lactam complexes as chiral templates
SV Ley, LR Cox, B Middleton, JM Worrall
Tetrahedron
(1999)
55
Chemical synthesis of the N-glycans of gp63, the major surface glycoprotein from Leishmania mexicana amazonensis
A Düffels, SV Ley
Journal of the Chemical Society Perkin Transactions 1
(1999)
Clean five-step synthesis of an array of 1,2,3,4-tetra-substituted pyrroles using polymer-supported reagents
M Caldarelli, J Habermann, SV Ley
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
(1999)
Rapid Assembly of Oligosaccharides: Total Synthesis of a Glycosylphosphatidylinositol Anchor of Trypanosoma brucei.
DK Baeschlin, AR Chaperon, V Charbonneau, LG Green, SV Ley, U Lücking, E Walther
Angew Chem Int Ed Engl
(1999)
37
Tritiated dihydroazadirachtin binging to Schistocerca gregaria testes and Spodoptera Sf9 cells suggests a similar cellular mechanism of action for azadirachtin
AJ Mordue, AJ Nisbet, L Jennens, SV Ley, W Mordue
AZADIRACHTA INDICA A. JUSS.
(1999)
Chemistry of Insect Antifeedants from Azadirachta indica (Part 22): Functionalisation of the Decalin Fragment of Azadirachtin via a Claisen Rearrangement Reaction
SV Ley*, CE Gutteridge, AR Pape, CD Spilling, C Zumbrunn
Synlett
(1999)
1999
Recent studies on the use of MPA and MTPA in the determination of the absolute configuration of secondary alcohols by 1H NMR
SK Latypov, JM Seco, E Quinoa, R Riguera, E Fernandez-Megia, SV Ley
Chemtracts
(1999)
12

Research Group

Telephone number

01223 336398

Email address