Publications

2011 - 2016

  • Shaya, J., Fontaine-Vive, F., Michel, B. Y., and Burger, A. (2016) Rational design of push-pull fluorene dyes : synthesis and structure-photophysics relationship. Chem. Eur. J., Accepted DOI : 10.1002/chem.201600581.
  • Barthes, N. P. F., Gavvala, K., Dziuba, D., Bonhomme, D., Karpenko, I. A., Dabert-Gay, A. S., Debayle, D., Demchenko, A. P., Benhida, R., Michel, B. Y., Mely, Y., and Burger, A. (2016) Dual emissive analogue of deoxyuridine as a sensitive hydration-reporting probe for discriminating mismatched from matched DNA from DNA/DNA and DNA/RNA duplexes. J. Mater. Chem. C, 4, 3010–3017.
  • Michel, B. Y., Cuendet, M., Barthes, N. P. F., Burger, A., Bertrand, P., and Martinet, N. (2015) Détection des modifications de la méthylation de l’ADN et de la chromatine. Rev. Franc. Lab., 2015, 55–62.
  • Barthes, N. P. F., Karpenko, I. A., Spadafora, M., Auffret, J., Demchenko, A. P., Mely, Y., Benhida, R., Michel, B. Y., Burger, A., and Dziuba, D. (2015) Development of environmentally sensitive fluorescent and dual emissive deoxyuridine analogues. RSC Adv., 5, 33536–33545.
  • Dziuba, D., Karpenko, I. A., Barthes, N. P. F., Michel, B. Y., Klymchenko, A. S., Benhida, R., Demchenko, A. P., Mely, Y., and Burger, A. (2014) Rational Design of a Solvatochromic Fluorescent Uracil Analogue with a Dual‐Band Ratiometric Response Based on 3‐Hydroxychromone. Chem. Eur. J., 20, 1998–2009.
  • Kuznetsova, A. A., Kuznetsov, N. A., Vorobjev, Y. N., Barthes, N. P. F., Michel, B. Y., Burger, A., and Fedorova, O. S. (2014) New environment-sensitive multichannel DNA fluorescent label for investigation of the protein-DNA interactions. PLoS ONE (Uversky, V. N., Ed.), 9, e100007.
  • Kenfack, C. A., Klymchenko, A. S., Duportail, G., Burger, A., and Mely, Y. (2012) Ab initio study of the solvent H-bonding effect on ESIPT reaction and electronic transitions of 3-hydroxychromone derivatives. Phys. Chem. Chem. Phys., 14, 8910–8918.
  • Dziuba, D., Postupalenko, V. Y., Spadafora, M., Klymchenko, A. S., Guérineau, V., Mely, Y., Benhida, R., and Burger, A. (2012) A universal nucleoside with strong two-band switchable fluorescence and sensitivity to the environment for investigating DNA interactions. J. Am. Chem. Soc., 134, 10209–10213.
  • Martinet, N., Michel, B. Y., Bertrand, P., and Benhida, R. (2012) Small molecules DNA methyltransferases inhibitors. MedChemComm 3, 263–273.
  • Dziuba, D., Benhida, R., and Burger, A. (2011) A Mild and Efficient Protocol for the Protection of 3-Hydroxychromones Under Phase-Transfer Catalysis. Synthesis, 2011, 2159–2164.
  • Krishnakumar, K. S., Michel, B. Y., Nguyen-Trung, N. Q., Fenet, B., and Strazewski, P. (2011) Intrinsic pKa values of 3’-aminoacyl-3’-deoxyadenosines determined by pH dependent 1H NMR in H2O. Chem. Commun., 47, 3290–3292.
  • Theodorakopoulos, N., Govetto, B., Industry, B., Massi, L., Gaysinski, M., Deleury, E., Mura, C., Marais, A., Arbiol, G., Burger, A., Gorges, M., Panabières, F., Ponchet, M., and Galiana, E. (2011) Biology and ecology of biofilms formed by a plant pathogen Phytophthora parasitica : from biochemical ecology to ecological engineering. Procedia Environmental Sciences, 9, 178-182.

Antérieures à 2011

  • Safadi, El, Y., Paillart, J.-C., Laumond, G., Aubertin, A.-M., Burger, A., Marquet, R., and Vivet-Boudou, V. (2010) 5-Modified-2′-dU and 2′-dC as Mutagenic Anti HIV-1 Proliferation Agents : Synthesis and Activity. J. Med. Chem., 53, 1534–1545.
  • Spadafora, M., Postupalenko, V. Y., Shvadchak, V. V., Klymchenko, A. S., Mely, Y., Burger, A., and Benhida, R. (2009) Efficient Synthesis of Ratiometric Fluorescent Nucleosides Featuring 3-Hydroxychromone Nucleobases. Tetrahedron, 65, 7809–7816.
  • Spadafora, M., Mehiri, M., Burger, A., and Benhida, R. (2008) Friedel–Crafts and modified Vorbrüggen ribosylation. A short synthesis of aryl and heteroaryl-C-nucleosides. Tet. Lets., 49, 3967–3971.
  • Ben Gaied, N., Glasser, N., Ramalanjaona, N., Beltz, H., Wolff, P., Marquet, R., Burger, A., and Mely, Y. (2005) 8-vinyl-deoxyadenosine, an alternative fluorescent nucleoside analog to 2′-deoxyribosyl-2-aminopurine with improved properties. Nucleic Acids Res., 33, 1031–1039.