En poursuivant votre navigation, vous acceptez l'utilisation de cookies destinés à améliorer la performance de ce site et à vous proposer des services et contenus personnalisés.

X

Publications 2020

To access the publications in open access, please click on the icon following the title of the article.


15. Laboratory scale UV–visible degradation of acetamiprid in aqueous marketed mixtures - Structural elucidation of photoproducts and toxicological consequences.
Nicol, E.; Varga, Z.; Vujovic, S.; Bouchonnet, S.
Chemosphere 2020, 248, 126040.
https://doi.org/10.1016/j.chemosphere.2020.126040
14. Base-assisted intramolecular C–N coupling reaction from NH2-bound cyclopalladated L-phenylalanine to indoline-2-carboxylic acid.
Jacquin-Labarre, A.; Coufourier, S.; Tamion, R.; Le Foll, A.; Levacher, V.; Afonso, C.; Gandon, V.; Journot, G.; Brière, J.-F.; Hoarau, C.
Organometallics 2020, 39 (5), 767-773.
https://doi.org/10.1021/acs.organomet.0c00030
13. Tridentate NNN ligand associating amidoquinoline and iminophosphorane: synthesis and coordination to Pd and Ni centers.
Mazaud, L.; Tricoire, M.; Bourcier, S.; Cordier, M.; Gandon, V.; Auffrant, A.
Organometallics 2020, 39 (5), 719-728.
https://doi.org/10.1021/acs.organomet.9b00867
12. Superelectrophilic gallium(III) homodimers in gallium chloride mediated methylation of benzene: a theoretical study.
Yang, S.; Bour, C.; Gandon, V.
ACS Catal. 2020, 10 (5), 3027-3033.
https://doi.org/10.1021/acscatal.9b05509
11. Tethered counterion-directed catalysis: merging the chiral ion-pairing and bifunctional ligand strategies in enantioselective gold(I) catalysis.
Zhang, Z.; Smal, V.; Retailleau, P.; Voituriez, A.; Frison, G.; Marinetti, A.; Guinchard, X.
J. Am. Chem. Soc. 2020, 142 (8), 3797-3805.
https://doi.org/10.1021/jacs.9b11154
10. An unconventional sulfur-to-selenium-to-carbon radical transfer: chemo-and regioselective cyclization of yne-ynamides.
Dutta, S.; Prabagar, B.; Vanjari, R.; Gandon, V.; Sahoo, A. K.
Green Chem. 2020, 22 (4), 1113-1118.
http://dx.doi.org/10.1039/C9GC03745D
9. Cryo-EM study of an archaeal 30S initiation complex gives insights into evolution of translation initiation. 
Coureux, P.-D.; Lazennec-Schurdevin, C.; Bourcier, S.; Mechulam, Y.; Schmitt, E.
Commun. Biol. 2020, 3 (1), 58.
https://doi.org/10.1038/s42003-020-0780-0
8. Use of β3-methionine as an amino acid substrate of Escherichia coli methionyl-tRNA synthetase.
Nigro, G.; Bourcier, S.; Lazennec-Schurdevin, C.; Schmitt, E.; Marlière, P.; Mechulam, Y.
J. Struct. Biol. 2020, 209 (2), 107435.
https://doi.org/10.1016/j.jsb.2019.107435
7. Aerosol synthesis of thermally stable porous noble metals and alloys by using bi-functional templates.
Odziomek, M.; Bahri, M.; Boissière, C.; Sanchez, C.; Lassalle-Kaiser, B.; Zitolo, A.; Ersen, O.; Nowak, S.; Tard, C.; Giraud, M.; Faustini, F.; Peron, J.
Mater. Horiz. 2020, 7 (2), 541-550.
http://dx.doi.org/10.1039/C9MH01408J
6. Photodegradation of benzisothiazolinone: Identification and biological activity of degradation products.
Varga, Z.; Nicol, E.; Bouchonnet, S.
Chemosphere 2020240, 124862.
https://doi.org/10.1016/j.chemosphere.2019.124862
5. Formal [8+3]-annulation between azaoxyallyl cations and tropones.
Force, G.; Pérot, A.; Guillot, R.; Gandon, V.; Leboeuf, D.
Synthesis 2020, 52 (04), 553-564.
http://dx.doi.org/10.1055/s-0039-1690745
4. Enantioselective synthesis of complex fused heterocycles through chiral phosphoric acid catalyzed intramolecular inverse-electron-demand aza-Diels–Alder reactions.
Jarrige, L.; Gandon, V.; Masson, G.
Chem. Eur. J. 2020, 26 (6), 1406-1413.
https://doi.org/10.1002/chem.201904902
3. Enantioselective total synthesis of cymoside through a bioinspired oxidative cyclization of a strictosidine derivative.
Dou, Y.; Kouklovsky, C.; Gandon, V.; Vincent, G.
Angew. Chem. Int. Ed. 2020, 59 (4), 1527-1531.
https://doi.org/10.1002/anie.201912812

2. Rational de novo design of a Cu-metalloenzyme for superoxide dismutation.
Mathieu, E.; Tolbert, A. E.; Koebke, K. J.; Tard, C.; Iranzo, O.; Penner-Hahn, J. E.; Policar, C.; Pecoraro, V. L.
Chem. Eur. J. 202026 (1), 249-258.
https://doi.org/10.1002/chem.201903808

1. Tracking monochloramine decomposition in MIMS analysis. 
Roumiguières, A.; Kinani, S.; Bouchonnet, S.
Sensors 202020 (1), 241.
https://doi.org/10.3390/s20010247