BSc, PhD (KC, London)
Chair in Pharmaceutical Industrial Chemistry
- About
-
- Email Address
- j.storey@abdn.ac.uk
- Telephone Number
- +44 (0)1224 272926
- Office Address
- Meston Room G106
- School/Department
- School of Natural and Computing Sciences
External Memberships
Head Chemist for TauRx Therapeutics
- Research
-
Research Overview
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.
Current Research
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.
Â
- Teaching
-
Teaching Responsibilities
Professor Storey teaches in the following courses:Â
- CM1010
- CM1011
- CM4017/CM3024 Honours/Advanced Chemistry
- CM5003 MChem Chemistry Applications
Â
- Publications
-
Page 1 of 16 Results 1 to 10 of 153
Molecular curvature and the twist-bend liquid crystal phases: the effect of the spacer
Liquid Crystals, pp. 1-8Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1080/02678292.2024.2373941
Liquid crystal trimers containing secondary amide groups
Liquid Crystals, pp. 1-10Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1080/02678292.2024.2382301
Liquid crystal dimers and the twist-bend phases: non-symmetric dimers consisting of mesogenic units of differing lengths
ChemPhysChem, vol. 25, no. 11, e202300848Contributions to Journals: ArticlesLETC inhibits α-Syn aggregation and ameliorates motor deficiencies in the L62 mouse model of synucleinopathy
European Journal of Pharmacology, vol. 970, 176505Contributions to Journals: ArticlesHeliconical nematic and smectic phases: the synthesis and characterisation of the CB4O.m and CB8O.m series
Liquid CrystalsContributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1080/02678292.2024.2334342
Ferroelectric nematogens containing a methylthio group
Materials Advances, vol. 5, no. 2, pp. 525-538Contributions to Journals: ArticlesThe influence of molecular shape and electronic properties on the formation of the ferroelectric nematic phase
Liquid CrystalsContributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1080/02678292.2024.2304598
A design approach to obtaining highly polar liquid crystal dimers
Liquid Crystals, vol. 51, no. 6, pp. 1035-1046Contributions to Journals: ArticlesCyanobiphenyl-based liquid crystal dimers and the twist-bend nematic phase: on the role played by the length and parity of the spacer
Liquid Crystals, vol. 51, no. 8-9, pp. 1446–1470Contributions to Journals: ArticlesThe Influence of the Imine Bond Direction on the Phase Behaviour of Symmetric and Non-symmetric Liquid Crystal Dimers
Journal of molecular liquids, vol. 391, no. Part A, 123226Contributions to Journals: Articles