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
Selective Acylation and Alkylation Reactions of Diols Using Dibutyltin Dimethoxide
Synlett
(1993)
1993
913
(doi: 10.1055/s-1993-22650)
Total synthesis of the spiroketal macrolide (+) milbemycin α1
Tetrahedron Letters
(1993)
34
7479
Microwave promoted hydrolysis of esters absorbed on alumina: A new deprotection method for pivaloyl groups
Synlett
(1993)
1993
793
(doi: 10.1055/s-1993-22612)
Synthesis of 4-Substituted Imidazoles via 4-Metallo Imidazole Intermediates
Synlett
(1993)
1993
748
(doi: 10.1055/s-1993-22594)
Dispiroketals in synthesis (part 4): Enantioselective desymmetrization of glycerol using a c2-symmetric disubstituted bis-dihydropyran.
Tetrahedron Letters
(1993)
34
5649
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 5): A new opportunity for oligosaccharide synthesis using differentially activated glycosyl donors and acceptors
Tetrahedron Letters
(1993)
34
8523
Chemistry of insect antifeedants from Azadirachta Indica (Part 15):1 Degradation studies of Azadirachtin leading to C8C14 bond cleavage.
Tetrahedron
(1993)
49
1675
Some Alkylation and Reductive Amination Studies of b-Ketomacrolides as Potential Metal Speciation Materials
Heterocycles
(1993)
35
263
(doi: 10.3987/com-92-s12)
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