Webster, Ruth - University of Bath - Department of Chemistry

个人简介

Following my MSci degree at the University of Strathclyde, I carried out my PhD under the supervision of Professor Robin Bedford at the University of Bristol.

研究领域

Metal insertion/activation of strong bonds Development of catalytic processes with traditionally inert bonds Design and implementation of simple chiral catalysts in enantioselective transformations Biopolymer synthesis New routes for metallopolymer synthesis

近期论文

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Espinal, M., Woof, C. R. and Webster, R., 2016. Iron catalyzed hydroboration:unlocking reactivity through ligand modulation. Chemistry - A European Journal, 22 (33), pp. 11605-11608. Gallagher, K., Espinal-Viguri, M., Mahon, M. and Webster, R., 2016. A study of two highly active, air-stable iron (III)-μ-oxo pre-catalysts:synthetic scope of hydrophosphination using phenyl- and diphenylphosphine. Advanced Synthesis & Catalysis King, A. K., Buchard, A., Mahon, M. F. and Webster, R. L., 2015. Facile, catalytic dehydrocoupling of phosphines using β-diketiminate iron(II) complexes. Chemistry - A European Journal, 21 (45), pp. 15960-15963. Brown, C. A., Nile, T. A., Mahon, M. F. and Webster, R. L., 2015. Iron catalysed Negishi cross-coupling using simple ethyl-monophosphines. Dalton Transactions, 44 (27), pp. 12189-12195. Gilmour, D. J., Webster, R. L., Perry, M. R. and Schafer, L. L., 2015. Titanium pyridonates for the homo- and copolymerization of rac-lactide and ε-caprolactone. Dalton Transactions, 44 (27), pp. 12411-12419. Bent, S. J., Mahon, M. F. and Webster, R. L., 2015. Copper malonamide complexes and their use in azide-alkyne cycloaddition reactions. Dalton Transactions, 44 (22), pp. 10253-10258. Bedford, R. B., Bowen, J. G., Davidson, R. B., Haddow, M. F., Seymour-Julen, A. E., Sparkes, H. A. and Webster, R. L., 2015. Facile hydrolysis and alcoholysis of palladium acetate. Angewandte Chemie-International Edition, 54 (22), pp. 6591-6594. Gallagher, K. and Webster, R. L., 2014. Room temperature hydrophosphination using a simple iron salen pre-catalyst. Chemical Communications, 50 (81), pp. 12109-12111. Evans, V., Mahon, M. F. and Webster, R. L., 2014. A mild, copper-catalysed amide deprotection strategy:use of tert-butyl as a protecting group. Tetrahedron, 70 (41), pp. 7593-7597. Tyler, S. N. G. and Webster, R. L., 2014. Sterically hindered malonamide monomers for the step growth synthesis of polyesters and polyamides. Chemical Communications, 50 (73), pp. 10665-10668. Webster, R. L., 2014. Random copolymerisations catalysed by simple titanium α-amino acid complexes. RSC Advances, 4 (10), pp. 5254-5260. Garcia, P., Payne, P. R., Chong, E., Webster, R. L., Barron, B. J., Behrle, A. C., Schmidt, J. A. R. and Schafer, L. L., 2013. Easily assembled, modular N,O-chelating ligands for Ta(V) complexation:A comparative study of ligand effects in hydroaminoalkylation with N-methylaniline and 4-methoxy-N-methylaniline. Tetrahedron, 69 (27-28), pp. 5737-5743. Webster, R. L., Noroozi, N., Hatzikiriakos, S. G., Thomson, J. A. and Schafer, L. L., 2013. Titanium pyridonates and amidates: novel catalysts for the synthesis of random copolymers. Chemical Communications, 49 (1), pp. 57-59. Bedford, R. B., Haddow, M. F., Mitchell, C. J. and Webster, R. L., 2011. Mild C-H halogenation of anilides and the isolation of an unusual palladium(I)-palladium(II) species. Angewandte Chemie, 123 (24), pp. 5638-5641. Bedford, R. B., Mitchell, C. J. and Webster, R. L., 2010. Solvent free catalytic C–H functionalisation. Chemical Communications, 46 (18), pp. 3095-3097. Bedford, R. B., Engelhart, J. U., Haddow, M. F., Mitchell, C. J. and Webster, R. L., 2010. Solvent-free aromatic C–H functionalisation/halogenation reactions. Dalton Transactions, 39 (43), pp. 10464-10472. Bedford, R. B., Webster, R. L. and Mitchell, C. J., 2009. Palladium-catalysed ortho-arylation of carbamate-protected phenols. Organic and Biomolecular Chemistry, 7 (23), pp. 4853-4857. Bedford, R. B., Haddow, M. F., Webster, R. L. and Mitchell, C. J., 2009. The catalytic ortho-arylation of tyrosine. Organic and Biomolecular Chemistry, 7 (15), pp. 3119-3127.