24. Coles, N. T.; Webster, R. L.* Iron Catalyzed Dehydrocoupling of Amine- and Phosphine-Boranes, Isr. J. Chem. 2017, DOI: 10.1002/ijch.201700018.

23. King, A. K.; Gallagher, K. J.; Mahon, M. F.; Webster, R. L.* Markovnikov versus anti-Markovnikov hydrophosphination: Divergent reactivity using an iron(II) β-diketiminate pre-catalyst, Chem. Eur. J. 2017, 23, 9039–9043.


22. Coles, N. T.; Mahon, M. F.; Webster, R. L.* Phosphine- and Amine-Borane Dehydrocoupling Using a Three-Coordinate Iron(II) β-Diketiminate Precatalyst, Organometallics 2017, 36, 2262–2268.

21. Webster, R. L.* β-Diketiminate complexes of the first row transition metals: applications in catalysis, Dalton Trans. 2017, 46, 4483-4498.


20. Espinal-Viguri, M.; Mahon, M. F.; Tyler, S. N. G.; Webster, R. L.* Iron catalysis for the synthesis of ligands: Exploring the products of hydrophosphination as ligands in cross-coupling, Tetrahedron 2017, 1, 64-69.


19. Espinal-Viguri, M.; King, A. K.; Lowe, J. P.; Mahon, M. F.; Webster, R. L.* Hydrophosphination of unactivated alkenes and alkynes using iron(II): catalysis and mechanistic insight, ACS Catal. 2016, 6, 7892-7897.

18. Espinal-Viguri, M.; Woof, C. R.; Webster, R. L.* Iron catalyzed hydroboration: unlocking reactivity through ligand modulation, Chem. Eur. J. 2016, 22, 11605–11608.

17. Gallagher, K. J.; Espinal-Viguri, M.; Mahon, M. F.; Webster, R. L.*A study of two highly active, air-stable iron (III)-μ-oxo pre-catalysts: synthetic scope of hydrophosphination using phenyl- and diphenylphosphine, Adv. Synth. Catal. 2016, 358, 2460-2468.

16. King, A. K.; Buchard, A.; Mahon, M. F.; Webster, R. L.* Facile, catalytic dehydrocoupling of phosphines using β-diketiminate iron(II) complexes, Chem. Eur. J. 2015, 21, 15960-15963.

15. Gilmour, D. J.; Webster, R. L.; Perry, M. R.; Schafer, L. L. Titanium pyridonates for the homo- and copolymerization of rac-lactide and ε-caprolactone, Dalton Trans. 2015, 44, 12411-12419.

14. Bent, S. J.; Mahon, M. F.; Webster, R. L.* Copper malonamide complexes and their use in azide-alkyne cycloaddition reactions, Dalton Trans. 2015, 44, 10253-10258.

13. Bedford, R. B.; Bowen, J. G.; Davidson, R. B.; Haddow, M. F.; Seymour-Julen, A. E.; Sparkes, H. A.; Webster R. L. Facile hydrolysis and alcoholysis of palladium acetate, Angew. Chem. Int. Ed. 2015, 54, 6591-6594.

12. Brown, C. A.; Nile, T. A.; Mahon, M. F.; Webster R. L.* Iron catalysed Negishi cross-coupling using simple ethyl-monophosphines, Dalton Trans. 2015, 44, 12189-12195.

11. Gallagher K. J.; Webster R. L.* Room temperature hydrophosphination using a simple iron salen pre-catalyst, Chem. Commun. 2014, 50, 12109-12111.

10. Evans V.; Mahon M. F.; Webster R. L.* A mild, copper-catalysed amide deprotection strategy: use of tert-butyl as a protecting group, Tetrahedron, 2014, 70, 7593-7597.


9. Tyler S. N. G.; Webster R. L.* Sterically hindered malonamide monomers for the step growth synthesis of polyesters and polyamides, Chem. Commun. 2014, 50, 10665-10668.


8. Webster R. L.* Random copolymerisations catalysed by simple titanium α-amino acid complexes, RSC Adv. 2014, 4, 5254-5260.


7. Garcia P.; Payne P. R.; Chong E.; Webster R. L.; Barron B. J.; Behrle A. C.; Schmidt J. A. R.; Schafer L. L. 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, 2013, 69, 5737-5743.

6.Webster R. L.; Noroozi N.; Hatzikiriakos S. G.; Thomson J. A.; Schafer L. L. Titanium pyridonates and amidates: novel catalysts for the synthesis of random copolymers, Chem. Commun. 2013, 49, 57-59.

5. Bedford R. B.; Haddow M. F.; Mitchell C. J.; Webster R. L. Mild C-H halogenation of anilides and the isolation of an unusual palladium(I)-palladium(II) species, Angew. Chem. Int. Ed. 2011, 50, 5524-5527.

4. Bedford R. B.; Mitchell C. J.; Webster R. L. Solvent free catalytic C–H functionalisation, Chem. Commun. 2010, 46, 3095-3097.

3. Bedford R. B.; Engelhart J. U.; Haddow M. F.; Mitchell C. J.; Webster R. L. Solvent-free aromatic C–H functionalisation/halogenation reactions, Dalton Trans. 2010, 39, 10464-10472.

2. Bedford R. B.; Webster R. L.; Mitchell C. J. Palladium-catalysed ortho-arylation of carbamate-protected phenols, Org. Biomol. Chem. 2009, 7, 4853-4857.

1. Bedford R. B.; Haddow M. F.; Webster R. L.; Mitchell C. J. The catalytic ortho-arylation of tyrosine, Org. Biomol. Chem. 2009, 7, 3119-3127.