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
Diastereoselective oxygen to carbon rearrangements of anomerically linked enol ethers and the total synthesis of (+)-(S,S)-cis-6-methyltetrahydropyran-2-ylacetic acid, a component of civet
– JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
(2000)
2385
(doi: 10.1039/b001243m)
The synthesis of mono- and bicyclic ethers via acid catalysed ring-opening cyclisation of tetrahyclropyranyl ether derivatives
– JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
(2000)
1829
(doi: 10.1039/a909302h)
The use of π-allyltricarbonyliron lactone complexes in the synthesis of the resorcylic macrolides α- and β-zearalenol
– JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
(2000)
3028
(doi: 10.1039/b005942k)
Methyl 2,3-O-(6,6′-octahydro-6,6′-bi-2h-pyran-2,2′-diyl)-α-d- galactopyranoside: α-D-Galactopyranoside, methyl, 2,3-O-octahydro[2,2′-bi-2H-pyran]-2,2′-diyl-, [2(2R,2′R)-]
– Organic Syntheses
(2000)
77,
212
Oxygen to carbon rearrangements of anomerically linked alkenols from tetrahydropyran derivatives: An investigation of the reaction mechanism via a double isotopic labelling crossover study
– Journal of the Chemical Society, Perkin Transactions 1
(2000)
1815
(doi: 10.1039/a909300a)
1,7-Asymmetric induction of chirality in a Mukaiyama aldol reaction using π-allyltricarbonyliron lactone complexes: highly diastereoselective synthesis of α-substituted β-hydroxy carbonyl compounds
– JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
(2000)
1677
(doi: 10.1039/b002056g)
Multi-step organic synthesis using solid-supported reagents and scavengers: A new paradigm in chemical library generation
– Journal of the Chemical Society, Perkin Transactions 1
(2000)
3815
(doi: 10.1039/b006588i)
A short stereoselective total synthesis of the fusarium toxin equisetin.
– Organic letters
(2000)
2,
3611
(doi: 10.1021/ol006493u)
The Total Synthesis of the Annonaceous Acetogenin, Muricatetrocin C
– Angewandte Chemie - International Edition
(2000)
39,
3622
The Total Synthesis of the Annonaceous Acetogenin, Muricatetrocin C
– Angewandte Chemie International Edition
(2000)
39,
3622
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