BSc, PhD (KC, London)
Chair in Pharmaceutical Industrial Chemistry
Head Chemist for TauRx Therapeutics
Free Radical Chemistry, Organic Methodology, Medicinal Chemistry
Our ability as organic chemists to develop new drugs to combat various diseases depends critically on understanding the behaviour of molecules and using this knowledge to prepare molecules efficiently. It is probably true to say that organic chemistry has reached a point where most molecules can be synthesised given sufficient resources. However, we are far from the position where this can be routinely accomplished in an efficient, atom economical, stereocontrolled and environmentally friendly manner. The major focus of my research effort is, therefore, the development of new synthetic methods and strategies in an attempt to meet some of these shortfalls.
An area that we are particularly interested in is the use of free radical reactions. Radical reactions offer the synthetic organic chemist a number of advantages, which include mild reaction conditions, high levels of regio control and significant functional group tolerance without the need to use protecting groups. We are interested in developing new methods of conducting radical reactions, the use of radical reactions in new bond forming processes and the use of radicals for the synthesis of biologically active compounds of medicinal significance.
Other research areas within the group include mechanistic studies in a variety of reactions, sugar chemistry with a view to the synthesis of biologically active fused carbosugars and tandem bond forming reaction protocols using organochromium compounds. We are also involved in a number of collaborative projects with the medical faculty.
Selected Current Projects
- Synthesis of biologically active fused pyridine, pyrimidine and pteridine heterocycles via radical translocation followed by cyclisation.
- A protecting group strategy for the synthesis of C-glycosides, disaccharides and fused carbosugars.
- Iodine atom transfer cyclisation as a route to a range of heterocyclic systems of biological significance.
- New methods of conducting and mediating radical reactions with an emphasis on the development of environmentally friendly systems.
- The use of organic molecules as asymmetric catalysts.
Professor Storey teaches in the following courses:Â
- CM4017/CM3024 Honours/Advanced Chemistry
- CM5003 MChem Chemistry Applications
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The influence of molecular shape and electronic properties on the formation of the ferroelectric nematic phaseLiquid CrystalsContributions to Journals: Articles
Liquid crystal dimers and the twist-bend phases: non-symmetric dimers consisting of mesogenic units of differing lengthsChemPhysChem, e202300848Contributions to Journals: Articles
The Influence of the Imine Bond Direction on the Phase Behaviour of Symmetric and Non-symmetric Liquid Crystal DimersJournal of molecular liquids, vol. 391, no. Part A, 123226Contributions to Journals: Articles
Ferroelectric nematogens containing a methylthio groupMaterials AdvancesContributions to Journals: Articles
To Be or Not To Be Polar: The Ferroelectric and Antiferroelectric Nematic PhasesACS Omega, vol. 8, no. 39, pp. 36562-36568Contributions to Journals: Articles
Exploring the Anti-Hypoxaemia Effect of Hydromethylthionine: A Prospective Study of Phase 3 Clinical Trial ParticipantsInternational Journal of Molecular Sciences, vol. 24, no. 18, 13747Contributions to Journals: Articles
Tailoring amide N-substitution to direct liquid crystallinity in benzanilide-based dimersJournal of molecular liquids, vol. 384, 122160Contributions to Journals: Articles
Can even-membered liquid crystal dimers exhibit the twist-bend nematic phase?: The preparation and properties of disulphide and thioether linked dimersLiquid CrystalsContributions to Journals: Articles
The Ferroelectric Nematic Phase: On the Role of Lateral Alkyloxy ChainsLiquid Crystals, vol. 50, no. 11-12, pp. 1960-1967Contributions to Journals: Articles
Molecular structure and the twist-bend nematic phase: the role of spacer length in liquid crystal dimersLiquid Crystals, vol. 50, no. 4, pp. 725-736Contributions to Journals: Articles