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

Total Synthesis of the Carboxylic Acid Ionophore Antibiotic CP-61,405 (Routiennocin)
N Kotecha*, S Ley, S Mantegani
Synlett
(1992)
1992
Microbial Oxidation in Synthesis: Preparation of Pseudo-α-D-glucopyranose from Benzene
S Ley*, L Yeung
Synlett
(1992)
1992
FURTHER REACTIONS OF TERT-BUTYL 3-OXOBUTANTHIOATE AND TERT-BUTYL 4-DIETHYL-PHOSPHONO-3-OXOBUTANTHIOATE - CARBONYL COUPLING REACTIONS, AMINATION, USE IN THE PREPARATION OF 3-ACYLTETRAMIC ACIDS AND APPLICATION TO THE TOTAL SYNTHESIS OF FULIGORUBIN-A
SV Ley, SC Smith, PR Woodward
Tetrahedron
(1992)
48
ENABLING METHODOLOGY - THE SYNTHETIC CHEMISTS CONTRIBUTION TO MOLECULAR RECOGNITION
SV LEY, LL YEUNG
MOLECULAR RECOGNITION : CHEMICAL AND BIOCHEMICAL PROBLEMS II
(1992)
111
Clerodane diterpenoids
AT Merritt, SV Ley
Natural product reports
(1992)
9
Dispiroketals in synthesis: Preparation of a stable, sterically demanding glyceraldehyde ketal and diastereoselective reactions with simple organometallic reagents
S Ley*, M Woods, A Zanotti-Gerosa
Synthesis
(1992)
1992
Chemistry of insect antifeedants from Azadirachta indica (part 13): on the use of the intramolecular Diels–Alder reaction for the construction of trans -fused hydrobenzofuran fragments for azadirachtin synthesis
HC Kolb, SV Ley, RN Sheppard, AMZ Slawin, SC Smith, DJ Williams, A Wood
Journal of the Chemical Society Perkin Transactions 1
(1992)
The use of π-allyltricarbonyliron lactone complexes in the synthesis of the β-lactone esterase inhibitor (−)-valilactone.
RW Bates, R Fernandez-Moro, SV Ley
Tetrahedron
(1991)
47
Synthesis of the alkaloids (−)-heliotridane and (−)-isoretronecanol via π-allyltricarbonyliron lactam complexes.
JG Knight, SV Ley
Tetrahedron Letters
(1991)
32
CHEMISTRY OF INSECT ANTIFEEDANTS FROM AZADIRACHTA-INDICA .2. CHARACTERIZATION AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF SOME NOVEL REARRANGED AZADIRACHTINS
SV Ley, JC Anderson, WM Blaney, ED Morgan, RN Sheppard, MSJ Simmonds, AMZ Slawin, SC Smith, DJ Williams, A Wood
Tetrahedron
(1991)
47

Research Group

Telephone number

01223 336398

Email address