Publications and Further Research Outputs
Peer-Reviewed Publications
Varghese S, Cotter M, Chevot F, Fergus C, Cunningham C, Mills KH, Connon SJ, Southern JM, Kelly VP. , In vivo modification of tRNA with an artificial nucleobase leads to full disease remission in an animal model of multiple sclerosis, Nucleic Acid Research, 45, (4), 2017, p2029 - 2039
S.J. Connon and J.M. Southern, 'Substituted Pyrimidine Derivatives useful in the Treatment of Autoimmune Diseases', Rouse, WO2016050804 (A1), 2016
David Mangan, Neasa McNabola, Emily H. Clark, Isabel Bermudez, Susan Wonnacott and J. Mike Southern, A new synthesis and preliminary evaluation of some analogues of mecamylamine - a compound with anti-addiction properties, Organic and Biomolecular Chemistry, 14, 2016, p10787 - 10798
Neasa McNabola, Cornelius J. O'Connor, Mark D. Roydhouse, Michael D. Wall, J. Mike Southern, A one-pot synthesis of 3-nitrothiophene and 3-nitro-2-substituted thiophenes, Tetrahedron, 71, (28), 2015, p4598 - 4603
Introduction to Aromatic Chemistry in, editor(s)Chris Rostron Jill Barber , Pharmaceutical Chemistry (Integrated Foundations of Pharmacy), Oxford University Press, 2013, [Mike Southern]
Michael Southern and David Mangan, Derivatives of Mecamylamine, 2013, WO2013026852 A2
O'Connor, CJ, Roydhouse, MD, Przybyl, AM, Wall, MD, Southern, JM, Facile Synthesis of 3-Nitro-2-substituted Thiophenes, JOURNAL OF ORGANIC CHEMISTRY, 75, (8), 2010, p2534-2538
Southern, J. Mike; O'Neil, Ian A.; Kearns, Peter, A concise synthesis of highly functionalised 4-thiosugar derivatives, Synlett, 14, 2008, p2158 - 2160
Preparation and reactions of iminophosphoranes and their synthetic applications in the aza-Wittig reaction. in, editor(s)P.J. Murphy , Organophosphorus Reagents A Practical Approach in Chemistry, Oxford University Press, 2004, pp151 - [J.Mike Southern and Ian A. O'Neil]
Ian A. O'Neil, J. Mike Southern, J. Chris Woolley and Heather Hobbs, The Synthesis of b-N-Tosylaminohydroxylamines via the Ring Opening of N-Tosylaziridines and Their Use in Reverse-Cope Cyclisations, Tetrahedron Letters, 42, 2001, p8243-
Ian A. O'Neil, Ed Cleator, J. Mike Southern and David J. Tapolczay, The Stereospecific Addition of Hydroxylamines to a,b-Unsaturated Sulfones, Nitriles and Nitro compounds, Tetrahedron Letters, 42, 2001, p8251-
Ian. A. O'Neil, Ed Cleator, J. Mike Southern, Neal Hone, David J. Tapolczay, The Synthesis of Polyhydroxylated Pyrrolidines Using a Reverse-Cope Cyclisation., Synlett, 2000, p1408-
Ian. A. O'Neil, Ed Cleator, J. Mike Southern, Neal Hone, David J. Tapolczay, The Synthesis of Chiral Functionalised Piperidines Using a Reverse-Cope Cyclisation: The Effect of Solvent on Diastereoselectivity, Synlett, 2000, p695-
Ian A. O'Neil and J. Mike Southern, The Synthesis of Functionalised b-Hydroxyhydroxylamines via the Ring Opening of Epoxides and Their Use in Reverse-Cope Cyclisations., Tetrahedron Letters, 39, 1998, p9089-
Ian A. O'Neil, Andrew J. Potter, J. Mike Southern, Alexander Steiner and James V. Barkley, Conformationally Defined Piperazine bis(N-Oxides) Bearing Amino Acid Side Chains., Chemical Communications, 1998, p2511-
Ian A. O'Neil and J. Mike Southern, A New Tin Mediated Pummerer Synthesis of Vinyl Stannanes., Synlett, 1997, p1165-
I. E. Markó, J. M. Southern and H. Adams, Towards the Total Synthesis of Manzamines. Rapid and Efficient Assembly of a Middle Core Model, Tetrahedron Letters, 33, 1992, p4657-
I. E. Markó, J. M. Southern and M. L. Kantam, Stoichiometric C-C Bond Formation Using Triorganothallium Reagents., Synlett, 1991, p235-
I. E. Markó and J. M. Southern, Triorganothallium Reagents in Organic Chemistry. 1. A Simple, Efficient and Versatile Preparation of Ketones from Acid Chlorides, Journal of Organic Chemistry, 55, 1991, p3368-
Research Expertise
Description
Our overall goal is to exploit synthetic chemistry to probe biological mechanisms in order to understand and provide treatment for disease. Neuronal nicotinic acetylcholine receptors are an extremely exciting set of ion channels that we are targeting by developing sub-type specific ligands. Areas of particular interest to us are: addiction, pain management, Parkinson's disease, Alzheimer's disease, Schizophrenia and anxiety. In another area we employ a slightly different approach. Rather than targeting specific group of receptors the focus is on the preparation of a diverse range of heterosugars, in which the endocyclic oxygen is replaced with another heteroatom e.g. sulphur, nitrogen or selenium. This class of compounds have exciting anti-viral, anti-cancer and anti-bacterial properties and they are also glycosidase inhibitors. The diseases we are targeting via this approach include Hepatitis C, HIV, avian flu, cancer, MRSA, drug resistant TB, diabetes (type 1 and type 2) and obesity. Other areas of interest include chiral alpha-oxy anions, chiral reactions of electron-rich alkenes and remote chiralityRecognition
Awards and Honours
Visiting Professor, Louvain-la-Neuve University, Belgium
Memberships
Chartered Chemist and Member of the Royal Society of Chemistry