Recent Publications

2021

  • C. Tresse, M. François-Heude, V. Servajean, R. Ravinder, C. Lesieur, L. Geiben, L. Jeanne-Julien, V. Steinmetz, P. Retailleau, E. Roulland, J. M. Beau, S. Norsikian.
    Total Synthesis of Tiacumicin B: Study of the Challenging β-Selective Glycosylations
    Chem. Eur. J. accepted

2020

  • G. Dejouy, K. Renault, Q. Bonnin, A. Chevalier, C. Michaudet, M. Picquet, I. E. Valverde, A. Romieu.
    Fluorogenic Enzyme-Triggered Domino Reactions Producing Quinoxalin-2(1H)-one-based Heterocycles
    Org. Lett. 2020, 22 (16), pp. 6494-6499
    DOI: 10.1021/acs.orglett.0c02287

 

  • S. Norsikian.
    Systems with One Bridgehead (Ring Junction) Nitrogen Atom: Four Extra 1-Heteroatoms 3:1 (2007-2018).
    Comprehensive Heterocyclic Chemistry IV2020
    DOI: 10.1016/B978-0-12-818655-8.00031-7

 

  • H. Yu, S. Carbonnel, S. Torabi, M. Griesmann, E. Bleek, Y. Tang, S. Buchka, V. Basso, M. Shindo, M., F.-D. Boyer, T.L. Wang, M. Udvardi, M. T. Waters, C. Gutjahr.
    Lotus japonicus karrikin receptors display divergent ligand-binding specificities and organ-dependent redundancy.
    PLOS Genetics, 2020, 16, e1009249
    DOI: 10.1371/journal.pgen.1009249

 

  • S. Struk, C. De Cuyper, A. Jacobs, L. Braem, A. Walton, A. De Keyser, S. Depuydt, L. D. Vu, I. De Smet, F.-D. Boyer, D. Eeckhout, G. Persiau, K. Gevaert, G. De Jaeger, S. Goormachtig.
    Unraveling the MAX2 Protein Network in Arabidopsis thaliana: Identification of the Protein Phosphatase PAPP5 as a Novel MAX2 Interactor
    Mol. Cell. Proteomics, 2020, mcp.RA119.001766
    DOI: 10.1074/mcp.RA119.001766

 

  • A. Del Vecchio, A. Talbot, F. Caille, A. Chevalier, A. Sallustrau, O. Loreau, G. Destro, F. Taran, D. Audisio.
    Carbon Isotope Labeling of Carbamates by Late-Stage [11C], [13C] and [14C] Carbon Dioxide Incorporation
    Chem. Commun. 2020, 56 (78), pp. 11677-11680
    DOI: 10.1039/D0CC05031H

 

  • Q. Taulera, D. Lauressergues, K. Martin, M. Cadoret, V. Servajean, F.-D. Boyer, S. Rochange.
    Initiation of arbuscular mycorrhizal symbiosis involves a novel pathway independent from hyphal branching
    Mycorrhiza 2020, 30 (4), pp. 491-501
    DOI: 10.1007/s00572-020-00965-9

 

  • S. Norsikian, C. Tresse, M. François-Eude, L. Jeanne-Julien, G. Masson, V. Servajean, G. Genta-Jouve, J. M. Beau, E. Roulland.
    Total Synthesis of Tiacumicin B: Implementing H-bond-Directed Acceptor Delivery for Highly Selective beta-Glycosylations
    Angew. Chem. Int. Ed., 2020, 59 (16), pp. 6612
    DOI: 10.1002/anie.202000231

2019

  • Lesur E., Baron A., Dietrich C., Buchotte M., Doisneau G., Urban D., Beau J.-M., Bayan N., Vauzeilles B., Guianvarc’h D., Bourdreux Y.
    First access to a mycolic acid-based bioorthogonal reporter for the study of the mycomembrane and mycoloyltransferases in corynebacteria
    Chem. Commun., 2019, 55 (87), pp. 13074
    DOI: 10.1039/C9CC05754D

 

  • de Saint Germain, A., Retailleau, P., Norsikian, S., Servajean, V., Pelissier, F., Steinmetz, V., Pillot, J.-P., Rochange, S., Pouvreau, J.-B., Boyer, F.-D.
    Contalactone, a contaminant formed during chemical synthesis of the strigolactone reference GR24 is also a strigolactone mimic.
    Phytochemistry, 2019, 168, 112112
    DOI: 10.1016/j.phytochem.2019.112112

 

  • Cabriel C., Bourg N., Jouchet P., Dupuis G., Leterrier C., Baron A., Badet-Denisot M.-A., Vauzeilles B., Fort E. Lévêque-Fort S.
    Combining 3D single molecule localization strategies for reproducible bioimaging
    Nature Communications2019, 10(1), pp.1980
    DOI: 10.1038/s41467-019-09901-8

 

  • Van Overtveld M., Braem L., Struk S., Kaczmarek A. M., Boyer F.-D., Van Deun R., Gevaert K., Goormachtig S., Heugebaert T. S. A. Stevens C. V.
    Design and visualization of second-generation cyanoisoindole-based fluorescent strigolactone analogs
    The Plant Journal2019, 98(1), pp.165-180
    DOI: 10.1111/tpj.14197

2018

  • Beau J.-M., Boyer F.-D., Norsikian S., Urban D., Vauzeilles B. Xolin A.
    Glycosylation: The Direct Synthesis of 2‐Acetamido‐2‐Deoxy‐Sugar Glycosides
    European Journal of Organic Chemistry2018, 42, pp5795-5814
    DOI: 10.1002/ejoc.201800735

 

  • Jeanne-Julien L., Masson G., Astier E., Genta-Jouve G., Servajean V., Beau J. M., Norsikian S. Roulland E.
    Study of the Construction of the Tiacumicin B Aglycone
    Journal of Organic Chemistry2018, 83(2), pp.921-929
    DOI: 10.1021/acs.joc.7b02909

 

  • Beneito-Cambra M., Gareil P., Badet B., Badet-Denisot M. A. Delaunay N.
    First investigations for the characterization of glucosamine-6-phosphate synthase by capillary electrophoresis
    J Chromatogr B Analyt Technol Biomed Life Sci2018, 1072, pp.130-135
    DOI: 10.1016/j.jchromb.2017.11.015

 

  • Struk S., Braem L., Walton A., De Keyser A., Boyer F.-D., Persiau G., De Jaeger G., Gevaert K. Goormachtig S.
    Quantitative Tandem Affinity Purification, an Effective Tool to Investigate Protein Complex Composition in Plant Hormone Signaling: Strigolactones in the Spotlight
    Front. Plant Sci.2018, 9
    DOI: 10.3389/fpls.2018.00528

 

  • Xolin A., Losa R., Kaid A., Tresse C., Beau J.-M., Boyer F.-D. Norsikian S.
    Stereocontrolled glycoside synthesis by activation of glycosyl sulfone donors with scandium(iii) triflate
    Org. Biomol. Chem.2018, 16(2), pp.325-335
    DOI: 10.1039/C7OB02792C

 

  • Bouchardy L., Rodriguez-Ruiz V., Bournaud C., Boyer F.-D., Toffano M., Judeinstein P. Vo-Thanh G.
    Novel Class of Reversible Chiral Ionic Liquids Derived from Natural Amino Acids: Synthesis and Characterization
    ChemistrySelect2018, 3(3), pp.958-962
    DOI: 10.1002/slct.201702708

 

  • Boutet-Mercey S., Perreau F., Roux A., Clavé G., Pillot J.-P., Schmitz-Afonso I., Touboul D., Mouille G., Rameau C. Boyer F.-D.
    Validated Method for Strigolactone Quantification by Ultra High-Performance Liquid Chromatography – “ Electrospray Ionisation Tandem Mass Spectrometry Using Novel Deuterium Labelled Standards
    Phytochemical Analysis2018, 29(1), pp.59-68
    DOI: 10.1002/pca.2714

2017

  • Rasmussen A., Hu Y., Depaepe T., Vandenbussche F., Boyer F.-D., Van Der Straeten D. Geelen D.
    Ethylene Controls Adventitious Root Initiation Sites in Arabidopsis Hypocotyls Independently of Strigolactones
    J. Plant Growth Regul.2017, 36(4), pp.897-911
    DOI: 10.1007/s00344-017-9692-8

 

  • Pollet R., Bonnet C. S., Retailleau P., DurandD P. Toth E.
    Proton Exchange in a Paramagnetic Chemical Exchange Saturation Transfer Agent from Experimental Studies and ab initio Metadynamics Simulation
    Inorg. Chem.2017, 56(8), pp.4317-4323
    DOI: 10.1021/acs.inorgchem.6b02773

 

  • Norsikian S., Beretta M., Cannillo A., Auvray M., Martin A., Retailleau P., Iorga B. I. Beau J. M.
    Stereoselective Synthesis of 1,2-trans-Diamines Using the Three-Component Borono-Mannich Condensation – Reaction Scope and Mechanistic Insights
    Eur. J. Org. Chem.2017, 2017(14), pp.1940-1951
    DOI: 10.1002/ejoc.201700089

 

  • Jeanne-Julien L., Masson G., Astier E., Genta-Jouve G., Servajean V., Beau J.-M., Norsikian S. Roulland E.
    Synthesis of a Tiacumicin B Protected Aglycone
    Org. Lett.2017, 19(15), pp.4006-4009
    DOI: 10.1021/acs.orglett.7b01744

 

  • Gouasmat A., Lemetais A., Solles J., Bourdreux Y. Beau J. M.
    Catalytic Iron(III) Chloride Mediated Site-Selective Protection of Mono- and Disaccharides and One Trisaccharide
    Eur. J. Org. Chem.2017, 23), pp.3355-3361
    DOI: 10.1002/ejoc.201700538

 

  • Berthelot N., Brossay A., Gasciolli V., Bono J.-J., Baron A., Beau J.-M., Urban D., Boyer F.-D. Vauzeilles B.
    Synthesis of lipo-chitooligosaccharide analogues and their interaction with LYR3, a high affinity binding protein for Nod factors and Myc-LCOs
    Org. Biomol. Chem.2017, 15(37), pp.7802-7812
    DOI: 10.1039/C7OB01201B

2016

  • J. He, C. S. Bonnet, S. V. Eliseeva, S. Lacerda, T. Chauvin, P. Retailleau, F. Szeremeta, B. Badet, S. Petoud*, E. Tóth* and P. Durand*
    Prototypes of Lanthanide(III) Agents Responsive to Enzymatic Activities in Three Complementary Imaging Modalities: Visible/Near-Infrared Luminescence, PARACEST-, and T1-MRI
    J. Am. Chem. Soc., 2016, 138, pp2913-2916
    DOI: 10.1021/jacs.5b12084

 

  • M. Dumont, A. Lehner, B. Vauzeilles, J. Malassis, A. Marchant, K. Smyth, B. Linclau, A. Baron, J. Mas Pons, C. T. Anderson, D. Schapman, L. Galas, J.-C. Mollet and P. Lerouge*
    Plant cell wall imaging by metabolic click-mediated labelling of rhamnogalacturonan II using azido 3-deoxy-D-manno-oct-2-ulosonic acid
    Plant J., 2016, 85, 437-447.
    DOI: 10.1111/tpj.13104

 

  • A. de Saint Germain, G. Clave, M.-A. Badet-Denisot, J.-P. Pillot, D. Cornu, J.-P. Le Caer, M. Burger, F. Pelissier, P. Retailleau, C. Turnbull, S. Bonhomme, J. Chory, C. Rameau and F.-D. Boyer*
    An histidine covalent receptor and butenolide complex mediates strigolactone perception
    Nat. Chem. Biol., 2016, 12, pp 787-794
    DOI: 10.1038/nchembio.2147

 

  • C. Matthys, A. Walton, S. Struk, E. Stes, F. D. Boyer, K. Gevaert and S. Goormachtig
    The Whats, the Wheres and the Hows of strigolactone action in the roots
    Planta, 2016, 243, pp1327-1337
    DOI: 10.1007/s00425-016-2483-9

2015

  • S. Norsikian, M. Beretta, A. Cannillo, A. Martin, P. Retailleau and J.-M. Beau
    Synthesis of enantioenriched 1,2-trans-diamines using the borono-Mannich reaction with N-protected α-amino aldehydes
    Chem. Commun., 2015, 51, pp9991-9994
    DOI: 10.1039/c5cc01716e

 

  • F. Clerc, Commerçon, A., Vauzeilles, B*
    Couplage chimique de biomolécules in cellulo et in vivo
    Actualité Chimique, 2015, 393-394, 24-30.

 

  • M. Lopez-Obando, Y. Ligerot, S. Bonhomme, F.-D. Boyer and C. Rameau
    Strigolactone biosynthesis and signaling in plant development
    Development, 2015, 142, pp3615-3619
    DOI: 10.1242/dev.120006