The Ball Research Group
School of Chemistry, University of Nottingham, UK
20. Zinc Phosphide.
Barber, T.; Ball,* L. T.
Encyclopedia of Reagents for Organic Synthesis. 2022.
19. 5,5-Dioxido-10H-dibenzo[b,e][1,4]thiabismin-10-yl 4-Methylbenzenesulfonate.
Ball,* L. T.
Encyclopedia of Reagents for Organic Synthesis. 2022.
18. Thiourea.
Campopiano, O.; St. Jean Jr, D. J.; Ball,* L. T.
Encyclopedia of Reagents for Organic Synthesis. 2022.
17. Phosphine-catalyzed aryne oligomerization: direct access to α,ω-bisfunctionalized oligo(ortho-arylenes).
Bürger, M.; Ehrhardt, N.; Barber, T.; Ball; L. T.; Namyslo, J. C.; Jones, P. G.; Werz,* D. B.
J. Am. Chem. Soc. 2021, 143, 16796.
16. Synthesis of tert-alkyl phosphines: preparation of di-(1-
adamantyl)phosphonium trifluoromethanesulfonate and
tri-(1-adamantyl)phosphine
Barber, T.; Ball,* L. T.
Org. Synth. 2021, 98, 289.
15. Bismuth(V)-mediated C–H arylation of phenols and naphthols
Senior, A.; Ball,* L. T.
Synlett. 2020, 32, 235.
Invited article; selected as cover art.
14. Kinetic analysis of domino catalysis: a case study on gold-catalyzed arylation
Ball, L. T.; Corrie, T. J. A.; Cresswell, A. J.; Lloyd-Jones*, G. C.
ACS Catal. 2020, 10, 10420.
13. Organobismuth redox manifolds: versatile tools for synthesis
Ruffell, K.; Ball,* L. T.
Trends Chem. 2020, 2, 867.
Invited article.
12. Expanding ligand space: preparation, characterization and synthetic applications of air-stable, odorless di-tert-alkylphosphine surrogates
Barber, T.; Argent, S. P.; Ball,* L. T.
ACS Catal. 2020, 10, 5454.
Highlighted: Org. Process Res. Dev. 2020, 24, 885.
11. Polyurethanes and polyallophanates via sequence-selective copolymerization of epoxides and isocyanates
Jurrat, M.; Pointer-Gleadhill, B.; Ball,* L. T.; Chapman,* A.; Adriaenssens,* L. V.
J. Am. Chem. Soc. 2020, 142, 8136.
10. Modular bismacycles for the selective C-H arylation of phenols and naphthols
Jurrat, M.; Maggi, L.; Lewis, W.; Ball,* L. T.
Nature Chem. 2020, 12, 260.
Highlighted: Nature Chem. 2020, 12, 223.
9. Synthesis of air-stable, odorless thiophenol surrogates via Ni-catalyzed C-S cross-coupling
Magné, V.; Ball,* L. T.
Chem. Eur. J. 2019, 25, 8903.
Hot paper.
8. Au-catalyzed biaryl coupling to generate 5- to 9-membered rings: turnover-limiting reductive elimination versus π-complexation
Corrie, T. J. A.; Ball, L. T.; Russell, C. A.; Lloyd-Jones*, G. C.
J. Am. Chem. Soc. 2017, 139, 245.
7. Self-control tames the coupling of reactive radicals
Lloyd-Jones*, G. C.; Ball*, L. T.
Science 2014, 345, 381.
6. Gold-catalyzed oxidative coupling of arylsilanes and arenes: origin of selectivity and improved precatalyst
Ball, L. T.; Lloyd-Jones*, G. C.; Russell*, C. A.
J. Am. Chem. Soc. 2014, 136, 254.
5. N,N-Diphospholylamines – a new family of ligand for highly active chromium-based selective ethene oligomerisation catalysts
Stennett, T. E.; Hey, T. W.; Ball, L. T.; Flynn, S. R.; Radcliffe, J. E.; McMullin, C. L.; Wingad R. L.; Wass* D. F.
ChemCatChem 2013, 5, 2946.
4. Gold-catalyzed direct arylation
Ball, L. T.; Lloyd-Jones*, G. C.; Russell*, C. A.
Science 2012, 337, 1644.
3. Application of the lithiation-borylation reaction to the rapid and enantioselective synthesis of the bisabolane family of sesquiterpenes
Aggarwal*, V. K.; Ball, L. T.; Carobene, S.; Connelly, R. L.; Hesse, M. J.; Partridge, B. M.; Roth, P.; Thomas, S. P.; Webster, M. P.
Chem. Commun. 2012, 48, 9230.
2. Gold-catalysed oxyarylation of styrenes, mono- and gem-disubstituted olefins facilitated by an iodine(III) oxidant
Ball, L. T.; Lloyd-Jones*, G. C.; Russell*, C. A.
Chem. Eur. J. 2012, 18, 2931.
1. Arylsilanes: application to gold-catalyzed oxyarylation of alkenes
Ball, L. T.; Green, M.; Lloyd-Jones*, G. C.; Russell*, C. A.
Org. Lett. 2010, 12, 4724.