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 last 10 years we have completed the total synthesis of 28 natural products including spongistatin 1 (anti-mitotic agent), rapamycin (immunosuppressant), thapsigargin (SERCA pumps inhibitor), azadirachtin (insect antifeedant) and bengazole A (fungicide), taking our group total to 150 completed total syntheses. In addition to our research on natural product synthesis, we also have a new state-of-the-art flow chemistry facility. 

For more detailed research information, group members and our publication list please see the group website.

Publications

Dispiroketals in synthesis (Part 12): Functionalised dispiroketals as new chiral auxiliaries; the synthesis of dihydroxylated dispiroketals in optically pure form
BCB BEZUIDENHOUDT, GH CASTLE, SV LEY
Tetrahedron Letters
(1994)
35
Chemistry of insect antifeedants from Azadirachta indica (Part 17): Synthesis of model compounds of azadirachtin. Unusual effect of remote substituents on the course of the oxidative ring contraction reaction.
RB GROSSMAN, SV LEY
Tetrahedron
(1994)
50
SELECTIVE ACYLATION AND ALKYLATION REACTIONS OF DIOLS USING DIBUTYLTIN DIMETHOXIDE (PG 913, 1993)
CJ BOONS, GH CASTLE, JA CLASE, P GRICE, SV LEY, C PINEL
SYNLETT
(1994)
Chemistry of insect antifeedants from Azadirachta indica (Part 16): Synthesis of several derivatives of azadirachtin containing fluorescent or immunogenic reporter groups
RB GROSSMAN, SV LEY
Tetrahedron
(1994)
50
Sexual development of malaria parasites is inhibited in vitro by the Neem extract Azadirachtin, and its semi-synthetic analogues
I Jones
FEMS Microbiology Letters
(1994)
120
Model studies towards the insect antifeedant Jodrellin A using an organoselenium mediated cyclization reaction
WM BLANEY, AC CUNAT, SV LEY, FJ MONTGOMERY, MSJ SIMMONDS
Tetrahedron Letters
(1994)
35
DISPIROKETALS IN SYNTHESIS .10 - FURTHER REACTIONS OF DISPOKE PROTECTED LACTATE AND GLYCOLATE ENOLATES
GJ BOONS, R DOWNHAM, KS KIM, SV LEY, M WOODS
Tetrahedron
(1994)
50
STUDIES TOWARDS THE TOTAL SYNTHESIS OF RAPAMYCIN - A CONVERGENT AND STEREOSELECTIVE SYNTHESIS OF THE C22-C32 CARBON FRAMEWORK
JC ANDERSON, SV LEY, SP MARSDEN
Tetrahedron Letters
(1994)
35
STUDIES TOWARDS THE TOTAL SYNTHESIS OF RAPAMYCIN - PREPARATION OF THE C10-C17 CARBON UNIT
SV LEY, J NORMAN, C PINEL
Tetrahedron Letters
(1994)
35
Studies towards the total synthesis of rapamycin: Preparation of the cyclohexyl C33C42 fragment and further coupling to afford the C22C42 carbon unit
C KOUKLOVSKY, SV LEY, SP MARSDEN
Tetrahedron Letters
(1994)
35

Telephone number

01223 336398

Email address