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
Synthesis of (±)warburganal
– Tetrahedron Letters
(1981)
22,
3909
Synthesis of euryfuran, valdiviolide, and confertifolin
– Tetrahedron Letters
(1981)
22,
4747
Synthesis of cinnamolide and polygodial
– Journal of the Chemical Society, Chemical Communications
(1981)
507
(doi: 10.1039/c39810000507)
An intramolecular Diels-Alder approach to the synthesis of the right hand half of the ionophore antibiotic X-14547A
– Tetrahedron Letters
(1981)
22,
361
(doi: 10.1016/0040-4039(81)80099-8)
Cyclisation reactions of alkenyl β-ketoesters involving a novel phenylseleno group migration
– Tetrahedron Letters
(1981)
22,
2601
The synthesis and Diels-Alder reactions of 2-prop-2-enylidene-1,3-dioxolan
– JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
(1981)
1582
(doi: 10.1039/p19810001582)
Synthesis of a trans-decalin as a potential insect antifeedant
– Chemical Communications
(1981)
1001
(doi: 10.1039/c39810001001)
A convenient preparation of 2-haloenones from enones using phenylselenium halides
– Tetrahedron Letters
(1981)
22,
3301
OXYGEN ATOM TRANSFER FROM IODYLBENZENE TO DIPHENYL DISELENIDE - A CONVENIENT METHOD FOR DEHYDROGENATION OF STEROIDAL 3-KETONES
– Journal of the Chemical Society, Chemical Communications
(1981)
1044
(doi: 10.1039/C39810001044)
Diaryl telluroxides as new mild oxidising reagents
– Tetrahedron
(1981)
37,
213
(doi: 10.1016/0040-4020(81)85057-0)
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