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 Perruthenate (PSP): Clean Oxidation of Primary Alcohols to Carbonyl Compounds Using Oxygen as Cooxidant
B Hinzen*
Synthesis
(1998)
1998
Diastereoselective anomeric oxygen to carbon rearrangements of silyl enol ether derivatives of lactols.
DJ Dixon*, SV Ley, EW Tate
Synlett
(1998)
1998
Anomeric Oxygen to Carbon Rearrangements of Alkynyl Tributylstannane Derivatives of Lactols
MF Buffet*, DJ Dixon, SV Ley, EW Tate
Synlett
(1998)
1998
One-pot synthesis of penta- and hepta-saccharides from monomeric mannose building blocks using the principles of orthogonality and reactivity tuning
L Green*, B Hinzen, SJ Ince, P Langer, SV Ley, SL Warriner
Synlett
(1998)
1998
Double diastereodifferentiation in the Mukaiyama aldol reactions of π-allyltricarbonyliron lactone complexes: 1,7- vs. 1,2-asymmetric induction
SV Ley, LR Cox, JM Worrall
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
(1998)
Tricarbonyliron complexes: an approach to acyclic stereocontrol
LR Cox, SV Ley
Chemical Society Reviews
(1998)
27
Enantioselective aldol reactions of α-unsubstituted enol ether derivatives catalyzed by a chiral Ti(IV) complex
SV Ley, LR Cox
Chemtracts
(1997)
10
Tetra-n-propylammonium perruthenate (TPAP)-catalysed oxidations of alcohols using molecular oxygen as a co-oxidant
R Lenz, SV Ley
Journal of the Chemical Society Perkin Transactions 1
(1997)
1,5-Asymmetric induction of chirality: highly diastereoselective synthesis of homoallylic tertiary alcohols by the Lewis acid-mediated addition of allylstannanes into ketones in the side-chain of pi-allyltricarbonyliron lactone complexes
SV Ley, LR Cox
Journal of the Chemical Society, Perkin Transactions 1
(1997)
1,5-Asymmetric induction of chirality: highly diastereoselective addition reactions of organoaluminium reagents into ketone groups in the side-chain of pi-allyltricarbonyliron lactone complexes
SV Ley, LR Cox, G Meek, K-H Metten, C Piqué, JM Worrall
Journal of the Chemical Society, Perkin Transactions 1
(1997)

Research Group

Telephone number

01223 336398

Email address