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 4): Enantioselective desymmetrization of glycerol using a c2-symmetric disubstituted bis-dihydropyran.
Tetrahedron Letters
(1993)
34
5649
CHEMISTRY OF INSECT ANTIFEEDANTS FROM AZADIRACHTA-INDICA .15. DEGRADATION STUDIES OF AZADIRACHTIN LEADING TO C8-C-14 BOND-CLEAVAGE
Tetrahedron
(1993)
49
1675
UPTAKE, RETENTION, METABOLISM AND EXCRETION OF [22,23-H-3(2)]DIHYDROAZADIRACHTIN IN SCHISTOCERCA-GREGARIA
Journal of Insect Physiology
(1993)
39
935
(doi: 10.1016/0022-1910(93)90003-A)
Dispiroketals in Synthesis (Part 3):1Selective Protection of Diequatorial Vicinal Diols in Carbohydrates
Synthesis
(1993)
1993
689
(doi: 10.1055/s-1993-25923)
Some Alkylation and Reductive Amination Studies of b-Ketomacrolides as Potential Metal Speciation Materials
Heterocycles
(1993)
35
263
(doi: 10.3987/com-92-s12)
Alfred bader [2]
Chemical and Engineering News
(1992)
70
2
Microbial Oxidation in Synthesis: Preparation of a Potential Insulin Mimic from Benzene
Synlett
(1992)
1992
997
(doi: 10.1055/s-1992-21561)
CHEMISTRY OF INSECT ANTIFEEDANTS FROM AZADIRACHTA-INDICA .12. USE OF SILICON AS A CONTROL ELEMENT IN THE SYNTHESIS OF A HIGHLY FUNCTIONALIZED DECALIN FRAGMENT OF AZADIRACHTIN
Journal of the Chemical Society, Perkin Transactions 1
(1992)
2735
(doi: 10.1039/P19920002735)
Chemistry of insect antifeedants from Azadirachta indica , Part 14: absolute configuration of azadirachtin
Journal of the Chemical Society, Chemical Communications
(1992)
1304
(doi: 10.1039/c39920001304)
Total synthesis of the ionophore antibiotic CP-61,405 (routiennocin)
Tetrahedron
(1992)
48
7899
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