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

Mukaiyama aldol reactions of π-allyltricarbonyliron lactone and lactam complexes bearing trimethylsilyl enol ether side-chains. Not just formal, but genuine 1,7 induction of chirality
SV Ley, B Middleton, JM Worrall
Chemical Communications
(1998)
A novel decomplexation of π-allyltricarbonyliron lactone complexes using borohydride reagents:: a new route to stereodefined acyclic 1,5-diols and 1,5,7-triols (pg 229, 1998)
SV Ley, S Burckhardt, LR Cox, JM Worrall
CHEMICAL COMMUNICATIONS
(1998)
Highly diasteroselective synthesis of beta-hydroxy carbonyl compounds using pi-allyltricarbonyliron lactone complexes: a formal 1,7-asymmetric induction of chirality in a Mukaiyama aldol reaction (pg 227, 1998)
SV Ley, LR Cox
CHEM COMMUN
(1998)
Highly diastereoselective synthesis of β-hydroxy carbonyl compounds using π-allyltricarbonyliron lactone complexes: A formal 1,7-asymmetric induction of chirality in a Mukaiyama aldol reaction
SV Ley
Chemical Communications
(1998)
A novel decomplexation of π-allyltricarbonyliron lactone complexes using borohydride reagents:: a new route to stereodefined acyclic 1,5-diols and 1,5,7-triols
SV Ley, JM Worrall
Chemical Communications
(1998)
Synthesis of isoxazolidines using polymer supported perruthenate (PSP)
B Hinzen, SV Ley
Journal of the Chemical Society, Perkin Transactions 1
(1998)
Tuning glycoside reactivity: New tool for efficient oligosaccharide synthesis
NL Douglas, SV Ley, U Lücking, SL Warriner
Journal of the Chemical Society, Perkin Transactions 1
(1998)
Anomeric Oxygen to Carbon Rearrangements of Alkynyl Tributylstannane Derivatives of Lactols
MF Buffet*, DJ Dixon, SV Ley, EW Tate
Synlett
(1998)
1998
Tricarbonyliron complexes: An approach to acyclic stereocontrol
LR Cox, SV Ley
Chemical Society Reviews
(1998)
27
Studies Towards the Synthesis of the C29-C51 Fragment of Altohyrtin A
E Fernandez-Megia*, N Gourlaouen, SV Ley, GJ Rowlands
Synlett
(1998)
1998

Research Group

Telephone number

01223 336398

Email address