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Titre de la publication Année Groupe de recherche
Candelon, N., Lastécouères, D., Diallo, A.K., Ruiz Aranzaes, J., Astruc, D., Vincent, J.M. (). A highly active and reusable copper(I)-tren catalyst for the "click" 1,3-dipolar cycloaddition of azides and alkynes. In Chemical Communications (Issue 6, p. 741-743). https://doi.org/10.1039/b716306a CSH
Astruc, D., Ornelas, C., Ruiz, J. (). Metallocenyl dendrimers and their applications in molecular electronics, sensing, and catalysis. In Accounts of Chemical Research (Vol. 41, Issue 7, p. 841-856). https://doi.org/10.1021/ar8000074 CSH
Ornelas, C., Aranzaes, J.R., Salmon, L., Astruc, D. (). "Click" dendrimers: Synthesis, redox sensing of Pd(OAc) 2, and remarkable catalytic hydrogenation activity of precise Pd nanoparticles stabilized by 1,2,3-triazole-containing dendrimers. In Chemistry A European Journal (Vol. 14, Issue 1, p. 50-64). https://doi.org/10.1002/chem.200701410 CSH
Aranzaes, J.R., Astruc, D. (). Simple synthesis of organo-iron complexes from iron-sandwich raw materials using visible light. In Inorganica Chimica Acta (Vol. 361, Issue 1, p. 1-4). https://doi.org/10.1016/j.ica.2007.07.030 CSH
Boisselier, E., Salmon, L., Ruiz, J., Astruc, D. (). How to very efficiently functionalize gold nanoparticles by "click" chemistry. In Chemical Communications (Issue 44, p. 5788-5790). https://doi.org/10.1039/b812249k CSH
Boisselier, E., Diallo, A.K., Salmon, L., Ruiz, J., Astruc, D. (). Gold nanoparticles synthesis and stabilization via new "clicked" polyethyleneglycol dendrimers. In Chemical Communications (Issue 39, p. 4819-4821). https://doi.org/10.1039/b808987f CSH
Diallo, A.K., Ornelas, C., Salmon, L., Aranzaes, J.R., Astruc, D. (). "Homeopathic" catalytic activity and atom-leaching mechanism in Miyaura-Suzuki reactions under ambient conditions with precise dendrimer-stabilized Pd nanoparticles. In Angewandte Chemie International Edition (Vol. 46, Issue 45, p. 8644-8648). https://doi.org/10.1002/anie.200703067 CSH
Astruc, D. (). Organometallic chemistry and catalysis. In Organometallic Chemistry and Catalysis (p. 1-608). https://doi.org/10.1007/978-3-540-46129-6 CSH
Nonier, M.F., Vivas, N., De Gaulejac, N.V., Pianet, I., Fouquet, E. (). A kinetic study of the reactions of (+)-catechin with aldehydes derived from toasted oak. In Journal of the Science of Food and Agriculture (Vol. 87, Issue 11, p. 2081-2091). https://doi.org/10.1002/jsfa.2968 CSH
Ornelas, C., Ruiz Aranzaes, J., Cloutet, E., Alves, S., Astruc, D. (). Click assembly of 1,2,3-triazole-linked dendrimers, including ferrocenyl dendrimers, which sense both oxo anions and metal cations. In Angewandte Chemie International Edition (Vol. 46, Issue 6, p. 872-877). https://doi.org/10.1002/anie.200602858 CSH
Lemo, J., Heuzé, K., Astruc, D. (). Efficient and recyclable dendritic Buchwald-type catalyst for the Suzuki reaction. In Chemical Communications (Issue 42, p. 4351-4353). https://doi.org/10.1039/b710289e CSH
Astruc, D. (). The olefin metathesis reactions in dendrimers. In Oil and Gas Science and Technology (Vol. 62, Issue 6, p. 787-797). https://doi.org/10.2516/ogst:2007055 CSH
Ruiz Aranzaes, J., Belin, C., Astruc, D. (). Assembly between gold-thiolate nanoparticles and the organometallic cluster [Fe(η5-C5H5)(μ3-CO)] 4 toward redox sensing of oxo-anions. In Chemical Communications (Issue 33, p. 3456-3458). https://doi.org/10.1039/b708466h CSH
Ornelas, C., Boisselier, E., Martinez, V., Pianet, I., Ruiz Aranzaes, J., Astruc, D. (). New water-soluble polyanionic dendrimers and binding to acetylcholine in water by means of contact ion-pairing interactions. In Chemical Communications (Issue 47, p. 5093-5095). https://doi.org/10.1039/b710391c CSH
Tarascou, I., Ducasse, M.A., Dufourc, E.J., Moskau, D., Fouquet, E., Laguerre, M., Pianet, I. (). Structural and conformational analysis of two native procyanidin trimers. In Magnetic Resonance in Chemistry (Vol. 45, Issue 2, p. 157-166). https://doi.org/10.1002/mrc.1938 CSH
Lacoste, E., Vaique, E., Berlande, M., Pianet, I., Vincent, J.M., Landais, Y. (). Benzimidazole-pyrrolidine/H+ (BIP/H+), a highly reactive organocatalyst for asymmetric processes. In European Journal of Organic Chemistry (Issue 1, p. 167-177). https://doi.org/10.1002/ejoc.200600664 CSH