Publications

Journal Articles

22. R. Tarrieu, I. Hernandez Delgado, F. Zinna, V. Dorcet, S. Colombel-Rouen, C. Crévisy, O. Baslé, J. Bosson, J. Lacour, Chem. Commun., 2021, 3793–3796. Hybrids of Cationic [4]Helicene and N-Heterocyclic Carbene as Ligands for Complexes Exhibiting (Chir)Optical Properties in the Far Red Spectral Window.
http://dx.doi.org/10.1039/D1CC00898F

21. J. Bosson, G. M. Labrador, C. Besnard, D. Jacquemin, J. Lacour, Angew. Chem. Int. Ed., 2021, 8733–8738. Chiral Near-Infrared Fluorophores by Self-Promoted Oxidative Coupling of Cationic Helicenes with Amines / Enamines.
https://doi.org/10.1002/anie.202016643

20. H. Li, R. Duwald, S. Pascal, S. Voci, C. Besnard, J. Bosson, L. Bouffier, J. Lacour and N. Sojic, Chem. Commun., 2020, 56, 9771–9774. Near-infrared electrochemiluminescence in water through regioselective sulfonation of diaza [4] and [6]helicene dyes.
http://dx.doi.org/10.1039/D0CC04156D

19. R. Duwald, J. Bosson, S. Pascal, S. Grass, F. Zinna, C. Besnard, L. Di Bari, D. Jacquemin, J. Lacour, Chem. Sci., 2020, 11, 1165–1169. Merging polyacenes and cationic helicenes: from weak to intense chiroptical properties in the far red region.
http://dx.doi.org/10.1039/C9SC05407C

18. G. M. Labrador, C. Besnard, T. Bürgi, A. I. Poblador-Bahamonde, J. Bosson, J. Lacour, Chem. Sci., 2019, 10, 7059–7067. Stereochemical significance of O to N atom interchanges within cationic helicenes: experimental and computational evidence of near racemization to remarkable enantiospecificity.
http://dx.doi.org/10.1039/C9SC02127B

17. Z. Jarolimova, J. Bosson, G. M. Labrador, J. Lacour, E. Bakker, Electroanal., 2018, 30, 1378–1385. Ion Transfer Voltammetry in Polyurethane Thin Films Based on Functionalised Cationic [6]Helicenes for Carbonate Detection.
https://doi.org/10.1002/elan.201800080

16. C. Bauer, R. Duwald, G. M. Labrador, S. Pascal, P. Moneva Lorente, J. Bosson, J. Lacour, J. D. Rochaix, Org. Biomol. Chem., 2018, 16, 919–923. Specific labeling of mitochondria of Chlamydomonas with cationic helicene fluorophores.
http://pubs.rsc.org/en/content/articlepdf/2018/ob/c7ob02906c

15. Z. Jarolimova, J. Bosson, G. M. Labrador, J. Lacour, E. Bakker, Electroanal., 2018, 30, 650–657. Ion Transfer Voltammetry at Thin Films Based on Functionalized Cationic [6]Helicenes.
https://doi.org/10.1002/elan.201700669

14. R. Duwald, S. Pascal, J. Bosson, S. Grass, C. Besnard, T. Bürgi and J. Lacour, Chem. Eur. J., 2017, 23, 13596–13601. Enantiospecific Elongation of Cationic Helicenes by Electrophilic Functionalization at Terminal Ends.
https://doi.org/10.1002/chem.201703441

13. H. Li, S. Voci, A. Wallabregue, C. Adam, G. M. Labrador, R. Duwald, I. Hernández Delgado, S. Pascal, J. Bosson, J. Lacour, L. Bouffier, N. Sojic, ChemElectroChem, 2017, 4, 1750–1756. Efficient Annihilation Electrochemiluminescence of Cationic Helicene Luminophores.
https://doi.org/10.1002/celc.201600906

12. H. Li, A. Wallabregue, C. Adam, G. M. Labrador, J. Bosson, L. Bouffier, J. Lacour, N. Sojic, J. Phys. Chem. C, 2017, 121, 785–792. Bright Electrochemiluminescence Tunable in the Near-Infrared of Chiral Cationic Helicene Chromophores.
http://pubs.acs.org/doi/pdfplus/10.1021/acs.jpcc.6b11831

11. J. Bosson, G. M. Labrador, S. Pascal, F.-A. Miannay, O. Yushchenko, H. Li, L. Bouffier, N. Sojic, R. C. Tovar, G. Muller, D. Jacquemin, A. D. Laurent, B. Le Guennic, E. Vauthey, J. Lacour, Chem. Eur. J., 2016, 22, 18394–18403. Physicochemical and Electronic Properties of Cationic [6]Helicenes: from Chemical and Electrochemical Stabilities to Far-Red (Polarized) Luminescence. Highlighted as Front Cover.
http://dx.doi.org/10.1002/chem.201603591

10. G. M. Labrador, J. Bosson, Z. S. Breitbach, Y. Lim, E. R. Francotte, R. Sabia, C. Villani, D. W. Armstrong, J. Lacour, Chirality, 2016, 28, 282–289. High-Performance Liquid Chromatographic Resolution of Neutral and Cationic Hetero[6]Helicenes.
https://doi.org/10.1002/chir.22579

9. C. Adam, A. Wallabregue, H. Li, J. Gouin, R. Vanel, S. Grass, J. Bosson, L. Bouffier, J. Lacour, N. Sojic, Chem. Eur. J., 2015, 21, 19243–19249. Electrogenerated Chemiluminescence of Cationic Triangulene Dyes: Crucial Influence of the Core Heteroatoms.
https://doi.org/10.1002/chem.201501738

8. J. Bosson, J. Gouin, J. Lacour, Chem. Soc. Rev., 2014, 43, 2824–2840. Cationic Triangulenes and Helicenes: Synthesis, Shemical Stability, Optical Properties and Extended Applications of these Unusual Dyes.
https://doi.org/10.1039/C3CS60461F

7. F. Torricelli, J. Bosson, C. Besnard, M. Chekini, T. Bürgi, J. Lacour, Angew. Chem. Int. Ed., 2013, 52, 1796–1800. Modular Synthesis, Orthogonal Post-Functionalization, Absorption and Chiroptical Properties of Cationic [6]Helicenes.
https://doi.org/10.1002/anie.201208926

6. J. Bosson, A. Poater, L. Cavallo, S. P. Nolan, J. Am. Chem. Soc., 2010, 132, 13146–13149. Mechanism of Racemization of Chiral Alcohols Mediated by 16-Electron Ruthenium Complexes.
https://pubs.acs.org/doi/10.1021/ja104961s

5. S. Gaillard, J. Bosson, R. S. Ramón, P. Nun, A. M. Slawin, S. P. Nolan, Chem. Eur. J., 2010, 16, 13729–13740. Development of Versatile and Silver-Free Protocols for Gold (I) Catalysis.
https://doi.org/10.1002/chem.201001688

4. J. Bosson, S. P. Nolan, J. Org. Chem., 2010, 75, 2039–2043. N-Heterocyclic Carbene – Ruthenium Complexes for the Racemization of Chiral Alcohols.
https://pubs.acs.org/doi/10.1021/jo1001005

3. R. S. Ramón, J. Bosson, S. Díez-González, N. Marion, S. P. Nolan, J. Org. Chem., 2010, 75, 1197–1202. Au/Ag-Cocatalyzed Aldoximes to Amides Rearrangement under Solvent- and Acid-free Conditions.
https://pubs.acs.org/doi/10.1021/jo902461a

2. P Belmont, J. Bosson, T. Godet, M. Tiano, Anti-Cancer Agents Med. Chem., 2007, 7, 139–169. Acridine and Acridone, Anti-Cancer Properties and Synthetic Methods: Where Are We Now?
https://www.eurekaselect.com/58771/article

1. T. Godet, J. Bosson, P. Belmont, Synlett, 2005, 18, 2786–2788. Efficient Based-Catalyzed 5-exo-dig Cyclization of Carbonyl Groups on Unactivated Alkynyl Quinolines: An Entry to Versatile Oxygenated Heterocycles Related to the Furoquinoline Alkaloids Family.
https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-2005-918953


Patents

2. P. O. Belmont, L. Meijer, P. Cohen, A. Patin, J. Bosson, P. G. Goekjian, Tetrahydrocyclopenta[c]acridine Derivatives as Kinase Inhibitors and Biological Applications Thereof. PCT Int. Appl. (2009), 37pp. WO 2009090623

1. P. O. Belmont, L. Meijer, P. Cohen, A. Patin, J. Bosson, P. G. Goekjian, Derivatives of Tetrahydrocyclopenta[c]acridines Inhibiting Kinases and Their Biological Applications. Fr. Demande (2009), 32pp. FR 2926550