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

Synthesis of High-Mannose Type Neoglycolipids: Active Targeting of Liposomes to Macrophages in Gene Therapy
A Düffels, LG Green, SV Ley, AD Miller
Chemistry (Weinheim an der Bergstrasse, Germany)
(2000)
6
Pinene-derived bipyridine ligands (PINDY) in asymmetric catalysis.
AV Malkov, IR Baxendale, M Bella, V Langer, P Kocovsky
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2000)
219
Polymer Supported Reagents in Synthesis: Preparation of Bicyclo[2.2.2]octane Derivatives via Tandem Michael Addition Reactions and Subsequent Combinatorial Decoration
SV Ley, A Massi
Journal of combinatorial chemistry
(2000)
2
Rapid assembly of oligosaccharides: 1,2-Diacetal-mediated reactivity tuning in the coupling of glycosyl fluorides
DK Baeschlin, LG Green, MG Hahn, B Hinzen, SJ Ince, SV Ley
Tetrahedron: Asymmetry
(2000)
11
A short and efficient stereoselective synthesis of the polyhydroxylated macrolactone (+)-aspicillin
DJ Dixon, AC Foster, SV Ley
Org Lett
(2000)
2
Asymmetric molybdenum-catalyzed allylic substitution.
AV Malkov, P Spoor, V Vinader, P Kocovsky
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2000)
219
New strategies for organic catalysis: The first highly enantioselective organocatalytic Diels-Alder reaction
E Diez, SV Ley
Chemtracts
(2000)
13
Deracemization of Baylis-Hillman adducts
SV Ley, F Rodriguez
Chemtracts
(2000)
13
METHYL 2,3-O-(6,6'-OCTAHYDRO-6,6'-BI-2H-PYRAN-2,2'-DIYL)-a-D-GALACTOPYRANOSIDE
SV Ley, HMI Osborn
Organic Syntheses
(2000)
77
Tri-n-butyl[2-(trimethylsilyl)-ethoxymethoxymethyl]stannane: A convenient hydroxymethyl anion equivalent
E Fernández-Megía*, SV Ley
Synlett
(2000)
2000

Research Group

Telephone number

01223 336398

Email address