© 2019 by Ruth Webster

  • Twitter Social Icon
  • LinkedIn Social Icon

27. Webster, R. L.* 

 

Room Temperature Ni(II) Catalyzed Hydrophosphination and Cyclotrimerization of Alkynes

 

Inorganics20186, 120-131.

Invited Article for a Special Edition on First-Row Transition Metal Complexes.

28. Espinal-Viguri, M.; Neale, S. E.; Coles, N. T.; Macgregor. S. A.*; Webster, R. L.* 

 

Room temperature iron-catalyzed transfer hydrogenation and regioselective deuteration of carbon-carbon double bonds

 

J. Am. Chem. Soc. 2019, 141, 572-582.

26. Coles, N. T.; Mahon. F.; Webster, R. L.* 

 

1,1-Diphosphines and divinylphosphines via base catalyzed hydrophosphination

 

Chem. Commun. 201854, 10443-10446.

25. Provis-Evans, C. B.; Emanuelsson, E. A. C.; Webster, R. L.* 

 

Rapid metal-free formation of free-phosphines from phosphine oxides

 

Adv. Synth. Catal2018360, 3999-4004.

24. Coles, N. T.; Webster, R. L.* 

 

Iron Catalyzed Dehydrocoupling of Amine- and Phosphine-Boranes

 

Isr. J. Chem201757, 1070-1081.

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. 201723, 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, 201736, 2262–2268.

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 20171, 64-69.

21. Webster, R. L.*

 

β-Diketiminate complexes of the first row transition metals: applications in catalysis

 

Dalton Trans201746, 4483-4498.

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. 20166, 7892-7897.

18. Espinal-Viguri, M.; Woof, C. R.; Webster, R. L.

 

Iron catalyzed hydroboration: unlocking reactivity through ligand modulation

 

Chem. Eur. J. 201622, 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. 201521, 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-caprolactoneDalton Trans201544, 12411-12419.

14. Bent, S. J.; Mahon, M. F.; Webster, R. L.* 

 

Copper malonamide complexes and their use in azide-alkyne cycloaddition reactions

 

Dalton Trans201544, 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 acetateAngew. Chem. Int. Ed201554, 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 Trans201544, 12189-12195.

11. Gallagher K. J.; Webster R. L.

 

Room temperature hydrophosphination using a simple iron salen pre-catalyst

 

Chem. Commun. 201450, 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

 

Tetrahedron201470, 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. 201450, 10665-10668.

8. Webster R. L.* 

 

Random copolymerisations catalysed by simple titanium α-amino acid complexes

 

RSC Adv. 20144, 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-methylanilineTetrahedron201369, 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. 201349, 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. 201150, 5524-5527.

4. Bedford R. B.; Mitchell C. J.; Webster R. L. Solvent free catalytic C–H functionalisation, Chem. Commun. 201046, 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 Trans201039, 10464-10472.

2. Bedford R. B.; Webster R. L.; Mitchell C. J. Palladium-catalysed ortho-arylation of carbamate-protected phenolsOrg. Biomol. Chem2009, 7, 4853-4857.

1. Bedford R. B.; Haddow M. F.; Webster R. L.; Mitchell C. J. The catalytic ortho-arylation of tyrosineOrg. Biomol. Chem2009, 7, 3119-3127.