13. Sowiński, M. P.; Warnke, A.-L.; Lund, B. A.; Skagseth, S.; Cordes, D. B.; Lovett, J. E.; Haugland, M. M. Spirocyclic pyrrolidinyl nitroxides with exo-methylene substituents. ChemPlusChem 2024, Accepted Article. https://doi.org/10.1002/cplu.202400387 Data available: https://doi.org/10.18710/PIZ7H1.

12. Baussière, F.; Haugland, M. M. Radical Group Transfer of Vinyl and Alkynyl Silanes Driven by Photoredox Catalysis. J. Org. Chem. 2023, 88, 12451–12463. https://doi.org/10.1021/acs.joc.3c01213 Data available: https://doi.org/10.18710/U5RNGE. Featured in Org. Chem. Highlights!

11. Sowiński, M. P.; Gahlawat, S.; Lund, B. A.; Warnke, A.-L.; Hopmann, K. H.; Lovett, J. E.; Haugland, M. M. Conformational tuning improves the stability of spirocyclic nitroxides with long paramagnetic relaxation times. Commun. Chem. 2023, 6, 111. https://doi.org/10.1038/s42004-023-00912-7 Data available: https://doi.org/10.18710/UQMMZE

10. Hira, J.; Uddin, J. Md.; Haugland, M. M.; Lentz, C. S. From Differential Stains to Next Generation Physiology: Chemical Probes to Visualize Bacterial Cell Structure and Physiology. Molecules 2020, 25, 4949. https://doi.org/10.3390/molecules25214949

Pre-UiT:

9. Amaral, M.; Asiki, H.; Sear, C. E.; Singh, S.; Pieper, P.; Haugland, M. M.; Anderson, E. A.; Tempone, A. G. Biological activity and structure-activity relationship of dehydrodieugenol B analogues against visceral leishmaniasis. RSC Med. Chem. 2023, 14, 1344–1350. https://doi.org/10.1039/D3MD00081H

8. McNamee, R. E.; Haugland, M. M.; Nugent, J.; Chan, R.; Christensen, K. E.; Anderson, E. A. Synthesis of 1,3-disubstituted bicyclo[1.1.0]butanes via direct bridgehead functionalization. Chem. Sci. 2021, 12, 7480–7485. https://doi.org/10.1039/D1SC01836A

7. Sear, C. E.; Pieper, P.; Amaral, M.; Romanelli, M. M.; Costa-Silva, T. A.; Haugland, M. M.; Tate, J. A.; Lago, J. H. G.; Tempone, A. G.; Anderson, E. A. Synthesis and Structure–Activity Relationship of Dehydrodieugenol B Neolignans against Trypanosoma cruzi. ACS Infect. Dis. 2020, 6, 2872–2878. https://doi.org/10.1021/acsinfecdis.0c00523

6. Hardwick, J. S.; Haugland, M. M.; El-Sagheer, A. H.; Ptchelkine, D.; Beierlein, F. R.; Lane, A. N.; Brown, T.; Lovett, J. E.; Anderson, E. A. 2′-Alkynyl spin-labelling is a minimally perturbing tool for DNA structural analysis. Nucleic Acids Res. 2020, 48, 2830-2840. https://doi.org/10.1093/nar/gkaa086

5. Haugland, M. M.; Borsley, S.; Cairns-Gibson, D. F.; Elmi, A.; Cockroft, S. L. Synthetically Diversified Protein Nanopores: Resolving Click Reaction Mechanisms. ACS Nano 2019, 13, 4101-4110. https://doi.org/10.1021/acsnano.8b08691

4. Borsley, S.; Haugland, M. M.; Oldknow, S.; Cooper, J. A.; Burke, M. J.; Scott, A.; Grantham, W.; Vallejo, J.; Brechin, E. K.; Lusby, P. J.; Cockroft, S. L. Electrostatic Forces in Field-Perturbed Equilibria: Nanopore Analysis of Cage Complexes. Chem 2019, 5, 1275-1292. https://doi.org/10.1016/j.chempr.2019.03.004

3. Haugland, M. M.; Lovett, J. E.; Anderson, E. A. Advances in the synthesis of nitroxide radicals for use in biomolecule spin labelling. Chem. Soc. Rev. 2018, 47, 668-680. https://doi.org/10.1039/C6CS00550K

2. Haugland, M. M.; Anderson, E. A.; Lovett, J. E. Tuning the properties of nitroxide spin labels for use in electron paramagnetic resonance spectroscopy through chemical modification of the nitroxide framework. In Electron Paramagnetic Resonance: Volume 25, The Royal Society of Chemistry: 2017; pp 1-34. https://doi.org/10.1039/9781782629436-00001

1. Haugland, M. M.; El-Sagheer, A. H.; Porter, R. J.; Peña, J.; Brown, T.; Anderson, E. A.; Lovett, J. E. 2′-Alkynylnucleotides: A Sequence- and Spin Label-Flexible Strategy for EPR Spectroscopy in DNA. J. Am. Chem. Soc. 2016, 138, 9069-9072. https://doi.org/10.1021/jacs.6b05421