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
Dispiroketals in synthesis (part 19)1: Dispiroketals as enantioselective and regioselective protective agents for symmetric cyclic and acyclic polyols.
Tetrahedron Asymmetry
(1995)
6
2403
(doi: 10.1016/0957-4166(95)00318-J)
Behavioural responses of locusts and Spodoptera littoralis to azadirachtin and azadirachtin analogues containing fluorescent and immunogenic reporter groups
Journal of Insect Physiology
(1995)
41
555
(doi: 10.1016/0022-1910(95)00014-L)
Dispiroketals in synthesis (Part 14): Functionalised dispiroketals as new chiral auxiliaries; highly stereoselective Michael additions to a bifunctional, C2- symmetrical chiral auxiliary
Tetrahedron Letters
(1994)
35
7455
(doi: 10.1016/0040-4039(94)85340-1)
DISPIROKETALS IN SYNTHESIS .13. FUNCTIONALIZED DISPIROKETALS AS NEW CHIRAL AUXILIARIES - HIGHLY STEREOSELECTIVE DIELS-ALDER REACTIONS USING A BIFUNCTIONAL, C-2-SYMMETRICAL CHIRAL AUXILIARY
Tetrahedron Letters
(1994)
35
7451
(doi: 10.1016/0040-4039(94)85339-8)
Dispiroketals in synthesis (Part 12): Functionalised dispiroketals as new chiral auxiliaries; the synthesis of dihydroxylated dispiroketals in optically pure form
Tetrahedron Letters
(1994)
35
7447
(doi: 10.1016/0040-4039(94)85338-X)
Dispiroketals in synthesis (Part 11): Concomitant enantioselective and regioselective protection of 2,5- dibenzoyl-myo-inositol
Tetrahedron Letters
(1994)
35
7443
(doi: 10.1016/0040-4039(94)85337-1)
SELECTIVE ACYLATION AND ALKYLATION REACTIONS OF DIOLS USING DIBUTYLTIN DIMETHOXIDE (PG 913, 1993)
SYNLETT
(1994)
764
Sexual development of malaria parasites is inhibited in vitro by the Neem extract Azadirachtin, and its semi-synthetic analogues
FEMS Microbiology Letters
(1994)
120
267
(doi: 10.1016/0378-1097(94)90482-0)
Model studies towards the insect antifeedant Jodrellin A using an organoselenium mediated cyclization reaction
Tetrahedron Letters
(1994)
35
4861
DISPIROKETALS IN SYNTHESIS .10 - FURTHER REACTIONS OF DISPOKE PROTECTED LACTATE AND GLYCOLATE ENOLATES
Tetrahedron
(1994)
50
7157
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