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

The synthesis and assay of radiolabelled benzene derivatives
NJ Hales, H Heaney, JH Hollinshead, SV Ley
Tetrahedron
(1995)
51
Tuning the Reactivity of Glycosides: Efficient One-pot Oligosaccharide Synthesis1
P Grice, S Ley*, J Pietruszka, H Priepke, E Walther
Synlett
(1995)
1995
CYCLOHEXANE-1,2-DIACETALS IN SYNTHESIS .3. TUNING THE REACTIVITY OF GLYCOSIDES - EFFICIENT ONE-POT OLIGOSACCHARIDE SYNTHESIS
P GRICE, SV LEY, J PIETRUSZKA, HWM PRIEPKE, EPE WALTHER
SYNLETT
(1995)
CHEMISTRY OF INSECT ANTIFEEDANTS FROM AZADIRACHTA-INDICA .19. A POTENTIAL RELAY ROUTE FOR THE SYNTHESIS OF AZADIRACHTIN
AA Denholm, L Jennens, SV Ley, A Wood
Tetrahedron
(1995)
51
BIOSYNTHESIS OF TETRONASIN .4. PREPARATION OF DEUTERIUM-LABELED C19-C26, C17-C26, C-11-C26 AND C3-C26 POLYKETIDE FRAGMENTS AS PUTATIVE BIOSYNTHETIC PRECURSORS OF THE IONOPHORE ANTIBIOTIC TETRONASIN (ICI-139603)
G-J Boons, JA Clase, IC Lennon, SV Ley, J Staunton
Tetrahedron
(1995)
51
Chemistry of insect antifeedants from Azadirachta Indica (part 18): Demethylation and methylation of the C-8 position of the decalin portion of azadirachtin
W-J Koot, SV Ley
Tetrahedron
(1995)
51
Synthesis of β-dimorphecolic acid exploiting highly stereoselective reduction of a side-chain carbonyl group in a π-allyltricarbonyliron lactone complex
SV Ley, G Meek
Chemical Communications
(1995)
Dispiroketals in synthesis (part 19)1: Dispiroketals as enantioselective and regioselective protective agents for symmetric cyclic and acyclic polyols.
R Downham, PJ Edwards, DA Entwistle, AB Hughes, KS Kim, SV Ley
Tetrahedron Asymmetry
(1995)
6
Behavioural responses of locusts and Spodoptera littoralis to azadirachtin and azadirachtin analogues containing fluorescent and immunogenic reporter groups
MSJ Simmonds, WM Blaney, RB Grossman, SV Ley
Journal of Insect Physiology
(1995)
41
Dispiroketals in synthesis (Part 13): Functionalised dispiroketals as new chiral auxiliaries; highly stereoselective diels-alder reactions using a bifunctional, C2- symmetrical chiral auxiliary
BCB Bezuidenhoudt, GH Castle, JV Geden, SV Ley
Tetrahedron Letters
(1994)
35

Research Group

Telephone number

01223 336398

Email address