Stephen G. Davies
Waynflete Professor of Chemistry
Department of Chemistry
University of Oxford
United Kingdom
Biography
Stephen Graham "Steve" Davies (born 24 February 1950) is a British chemist and the Waynflete Professor of Chemistry at the University of Oxford. Davies obtained his BA in 1973 from New College, Oxford and his D.Phil, in 1975 under the supervision of Gordon H. Whitham. He subsequently held an ICI Postdoctoral Fellowship working with Malcolm Green (1975-1977) and a NATO Fellowship working with Derek Barton (1977-1978) before joining the CNRS at Gif-sur-Yvette as Attaché de Recherche working with Hugh Felkin. In 1980 he returned to Oxford to take up a University Lectureship in Chemistry. He also founded Oxford Diversity Ltd (a combinatorial chemistry company). In 2003 he founded VASTox (Value Added Screening Technology Oxford) a zebrafish screening company. It floated on AIM in 2004 and has since acquired Dainolabs (zebrafish) and Dextra (a carbohydrate chemistry company) as well as the assets of MNL Pharma. In 2009 the zebrafish screening operations was acquired by Evotec for £0.5 Million.[8] In 1996, he became Professor of Chemistry[3] and in 2006, Waynflete Professor of Chemistry. Davies is founder and editor-in-chief for Tetrahedron: Asymmetry. Davies along with Malcolm Green and Michael Mingos have compiled a set of rules that summarize where nucleophilic additions will occur on pi ligands.
Research Interest
Davies research is concerned with investigations into a wide variety of topics including the development of new synthetic methodology, catalysis, mechanistic investigations, total synthesis and collaborative projects in medicinal chemistry, this includes new applications for the conjugate addition of enantiopure lithium amides, development of kinetic resolution processes for the preparation of functionalised molecular building blocks, new methods for nucleophilic fluorination, methodology for the chemoselective functionalisation of unsaturated amines at the olefin (rather than the nitrogen atom), and application of these methodologies to the total synthesis of natural products of biological significance (including pyrrolidines, piperidines, tropanes, pyrrolizidines, and imino- and aminosugars).
Publications
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Bataille CJ, Brennan MB, Byrne S, Davies SG, Durbin M, Fedorov O, Huber KV, Jones AM, Knapp S, Liu G, Nadali A. Thiazolidine derivatives as potent and selective inhibitors of the PIM kinase family. Bioorganic & Medicinal Chemistry. 2017 May 1;25(9):2657-65.
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Davies SG, Fletcher AM, Roberts PM, Thomson JE. Asymmetric Synthesis of Pyrrolizidines, Indolizidines and Quinolizidines via a Double Reductive Cyclisation Protocol. Synlett. 2017 Aug 8.
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Davies SG, Fletcher AM, Houlsby IT, Roberts PM, Thomson JE. Structural Revision of the Hancock Alkaloid (−)-Galipeine. The Journal of Organic Chemistry. 2017 Aug 15.
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Davies SG, Lee JA, Roberts PM, Thomson JE, Yin J. Solid state conformations of α, β-unsaturated hydroxamates derived from the ‘chiral Weinreb amide’auxiliary (S)-N-1-(1′-naphthyl) ethyl-O-tert-butylhydroxylamine. Tetrahedron: Asymmetry. 2017 Aug 14.