29. Synthesis of highly functionalized bismacycles via post-transmetallation modification of arylboronic acids

​

Sivanandan, S. T.; Owen, B.; Guiry, P. J.; Ball,* L. T.

​

J. Org. Chem. 2023, 88, 9730.

​

Among the most-read new articles of July 2023

28. Photochemically mediated ring expansion of indoles and pyrroles with chlorodiazirines: synthetic methodology and thermal hazard assessment

​

Joynson, B. W.; Cumming, G. C.; Ball,* L. T.

​

Angew. Chem. Int. Ed. 2023, e202305081.

​

Highlighted: Org. Proc. Res. Dev. 2023, asap.

27. Coaxial dielectric spectroscopy as an in-line process analytical technique for reaction monitoring

​

Dalligos, D. M.; Pilling,* M. J.; Dimitrakis,* G.; Ball,* L. T.

​

Org. Process Res. Dev. 2023, 27, 1094.

​

26. Skeletal editing: interconversion of arenes and heteroarenes

​

Joynson,* B. W.; K.; Ball,* L. T.

 

Helv. Chem. Acta 2023, 106, e202200182. 

​

Invited article (Bürgenstock special issue).

25. meta-Selective C–H arylation of phenols via regiodiversion of electrophilic aromatic substitution

​

Senior, A.; Ruffell, K.; Ball,* L. T.

 

Nature Chem. 2023, 15, 386.

​

Highlighted: Org. Proc. Res. Dev. 2023, 27, 383.

24. Modular synthesis of α,α-diaryl α-amino esters via Bi(V)-mediated arylation/SN2-displacement of Kukhtin–Ramirez intermediates

​

Calcatelli, A.; Denton, R. M.; Ball,* L. T.

 

Org. Lett. 2022, 24, 8002.

​

Highlighted: Synfacts 2023, 19, 0205.

23. Umpolung synthesis of pyridyl ethers by Bi(V)-mediated O‑arylation of pyridones

​

Ruffell, K.; Gallegos, L. C.; Ling, K. B.; Paton,* R. S.; Ball,* L. T.

 

Angew. Chem. Int. Ed. 2022, 61, e202212873.

22. Bismuth-mediated α-arylation of acidic diketones with ortho-substituted boronic acids

​

Ruffell, K.; Argent, S. P.; Ling, K. B.; Ball,* L. T.

 

Angew. Chem. Int. Ed. 2022, 61, e202210840.

​

Highlighted: Synfacts 2022, 18, 1220.

21. Generation of thiyl radicals from air-stable, odorless thiophenol surrogates: application to visible-light-promoted C–S cross-coupling

​

Swan, C.; Maggi, L.; Park, M.; Taylor, S.; Shepherd, W.; Ball,* L. T.

 

Synthesis 2022, 54, 3399.

​

Invited article (Bürgenstock: Future Stars in Chemistry).

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.

​

Highlighted: Synfacts 2021, 17, 1334.

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. 2021, 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. 

  Organic Chemistry Portal

  Synfacts 2020, 16, 553.

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.