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2016

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24. Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles. 
El Mamouni, E. H.; Cattoen, M.; Cordier, M.; Cossy, J.; Arseniyadis, S.; Ilitki, H.; El Kaim, L.
Chem. Commun. 2016, 52 (100), 14490-14493.
http://dx.doi.org/10.1039/C6CC08171A
23. Formation and determination of organohalogen by-products in water. Part III. Characterization and quantitative approaches.
Kinani, A.; Kinani, S.; Bouchonnet, S.
Trends Anal. Chem. 2016, 85, 295-305.
https://doi.org/10.1016/j.trac.2016.09.013
22. Formation and determination of organohalogen by-products in water. Part II. Sample preparation techniques for analytical approaches.
Kinani, A.; Kinani, S.; Bouchonnet, S.
Trends Anal. Chem. 201685, 281-294.
https://doi.org/10.1016/j.trac.2016.07.006
21. Formation and determination of organohalogen by-products in water. Part I. Discussing the parameters influencing the formation of organohalogen by-products and the relevance of estimating their concentration using the AOX (adsorbable organic halide) method.
Kinani, A.; Kinani, S.; Richard, B.; Lorthioy, M.; Bouchonnet, S.
Trends Anal. Chem. 2016, 85, 273-280.
https://doi.org/10.1016/j.trac.2016.06.008
20. Photodegradation of cyprodinil under UV–visible irradiation – chemical and toxicological approaches.
Nicol, E.; Chayata, H.; Genty, C.; Bouchonnet, S.; Bourcier, S.
Rapid Commun. Mass Spectrom. 2016, 30 (19), 2201-2211.
http://dx.doi.org/10.1002/rcm.7685
19. Cobalt-catalyzed oxidative homocoupling of arylzinc species.
Bourne-Branchu, Y.; Moncomble, A.; Corpet, M.; Danoun, G.; Gosmini, C.
Synthesis 2016, 48 (19), 3352-3356.
http://dx.doi.org/10.1055/s-0035-1562488
18. Synthesis of symmetrical diaryl ketones by cobalt-catalyzed reaction of arylzinc reagents with ethyl chloroformate.
Rérat, A.; Michon, C.; Agbossou-Niedercorn, F.; Gosmini, C.
Eur. J. Org. Chem. 2016, 2016 (26), 4554-4560.
http://dx.doi.org/10.1002/ejoc.201600738
17. Electron transfer in tetramethylbiphosphinine complexes of Cp*2Yb and Cp*2Sm. 
Jaoul, A.; Clavaguera, C.; Nocton, G.
New J. Chem. 2016, 40 (8), 6643-6649.
http://dx.doi.org/10.1039/C6NJ00527F
16. Cobalt-catalyzed reductive cross-coupling between benzyl chlorides and aryl halides.
Pal, S.; Chowdhury, S.; Rozwadowski, E.; Auffrant, A.; Gosmini, C.
Adv. Synth. Catal. 2016, 358 (15), 2431-2435.
http://dx.doi.org/10.1002/adsc.201600378
15. Cobalt-catalyzed Csp3 −Csp3 homocoupling.
Cai, Y.; Qian, X.; Gosmini, C.
Adv. Synth. Catal. 2016, 358 (15), 2427-2430.
http://dx.doi.org/10.1002/adsc.201600213
14. Dihydroanatoxin-a is biosynthesized from proline in cylindrospermum stagnale PCC 7417: isotopic incorporation experiments and mass spectrometry analysis.
Méjean, A.; Dalle, K.; Paci, G.; Bouchonnet, S.; Mann, S.; Pichon, V.; Ploux, O.
J. Nat. Prod. 2016, 79 (7), 1775-1782.
http://dx.doi.org/10.1021/acs.jnatprod.6b00189
13. Synthesis and characterization of 1,1′-diphosphaplumbocenes: oxidative ligand transfer reactions with divalent thulium complexes.
Jaroschik, F.; Momin, A.; Martinez, A.; Harakat, D.; Ricard, L.; Le Goff, X.-F.; Nocton, G.
Organometallics 2016, 35 (11), 2032-2038.
http://dx.doi.org/10.1021/acs.organomet.6b00313
12. Cascade metathesis reactions for the synthesis of taxane and isotaxane derivatives.
Ma, C.; Letort, A.; Aouzal, R.; Wilkes, A.; Maiti, G.; Farrugia, L. J.; Ricard, L.; Prunet, J.
Chem. Eur. J. 2016, 22 (20), 6891-6898.
http://dx.doi.org/10.1002/chem.201600592
11. Theoretical insight into the coordination number of hydrated Zn2+ from gas phase to solution.
Jana, C.; Ohanessian, G.; Clavaguéra, C.
Theor. Chem. Acc. 2016, 135 (5), 141.
https://doi.org/10.1007/s00214-016-1887-8
10. Stepwise hydration of 2-aminooxazole: theoretical insight into the structure, finite temperature behavior and proton-induced charge transfer.
Calvo, F.; Bacchus-Montabonel, M. C.; Clavaguéra, C.
J. Phys. Chem. A 2016, 120 (15), 2380-2389.
http://dx.doi.org/10.1021/acs.jpca.5b12392
9. Photodegradation of fluorene in aqueous solution: Identification and biological activity testing of degradation products.
Kinani, S.; Souissi, Y.; Kinani, A.; Vujović, S.; Aït-Aïssa, S.; Bouchonnet, S.
J. Chromatogr. A 2016, 1442, 118-128.
https://doi.org/10.1016/j.chroma.2016.03.012
8. Characterization of the ultraviolet–visible photoproducts of thiophanate-methyl using high performance liquid chromatography coupled with high resolution tandem mass spectrometry—Detection in grapes and tomatoes.
Chayata, H.; Lassalle, Y.; Nicol, É.; Manolikakes, S. M.; Souissi, Y.; Bourcier, S.; Gosmini, C.; Bouchonnet, S.
J. Chromatogr. A 2016, 1441, 75-82.
https://doi.org/10.1016/j.chroma.2016.02.078
7. Preparation, structural analysis, and reactivity studies of phosphenium dications. 
Tay, M. Q. Y.; Ilić, G.; Werner-Zwanziger, U.; Lu, Y.; Ganguly, R.; Ricard, L.; Frison, G.; Carmichael, D.; Vidović, D.
Organometallics 2016, 35 (4), 439-449.
http://dx.doi.org/10.1021/acs.organomet.5b00763
6. Direct synthesis of doubly deprotonated, dearomatised lutidine PNP Cr and Zr pincer complexes based on isolated K and Li ligand transfer reagents. 
Simler, T.; Frison, G.; Braunstein, P.; Danopoulos, A. A.
Dalton Trans. 2016, 45 (7), 2800-2804.
http://dx.doi.org/10.1039/C6DT00144K
5. A practical cobalt-catalyzed cross-coupling of benzylic zinc reagents with aryl and heteroaryl bromides or chlorides. 
Benischke, A. D.; Knoll, I.; Rerat, A.; Gosmini, C.; Knochel, P.
Chem. Commun. 2016, 52 (15), 3171-3174.
http://dx.doi.org/10.1039/C5CC10272C
4. Stereoselectivity of Michael addition of P(X)–H-type nucleophiles to cyclohexen-1-ylphosphine oxide: the case of base-selective transformation.
Jaklińska, M.; Cordier, M.; Stankevič, M.
J. Org. Chem. 2016, 81 (4), 1378-1390.
http://dx.doi.org/10.1021/acs.joc.5b02337
3. Palladium(II) complexes featuring a mixed phosphine-pyridine-iminophosphorane pincer ligand: synthesis and reactivity. 
Cheisson, T.; Auffrant, A.
Dalton Trans. 2016, 45 (5), 2069-2078.
http://dx.doi.org/10.1039/C5DT02789F
2. Chirality-dependent structuration of protonated or sodiated polyphenylalanines: IRMPD and ion mobility studies. 
Lepère, V.; Le Barbu-Debus, K.; Clavaguera, C.; Scuderi, D.; Piani, G.; Simon, A.-L.; Chirot, F.; MacAleese, L.; Dugourd, P.; Zehnacker, A.
Phys. Chem. Chem. Phys. 2016, 18 (3), 1807-1817.
http://dx.doi.org/10.1039/C5CP06768E

1. New Pd(II) hemichelates devoid of incipient bridging CO⋯Pd interactions. 
Werle, C.; Anstine, D. M.; Karmazin, L.; Bailly, C.; Ricard, L.; Djukic, J.-P.
Dalton Trans. 2016, 45 (2), 607-617.
http://dx.doi.org/10.1039/C5DT03648H