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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

查看导师最新文章 (温馨提示:请注意重名现象,建议点开原文通过作者单位确认)

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.

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