Laboratoire d'Innovation Moléculaire et Applications - LIMA - UMR7042

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The 1,2,3 Triazolo 1,5-a pyridine ring
BALLESTEROS-GARRIDO, Rafael, BONNAFOUX, Laurence, LEROUX, Frederic R., ABARCA, Belen et COLOBERT, Francoise, 2009. The 1,2,3 Triazolo 1,5-a pyridine ring: A sensitive sensor for the electronic pro. le of phosphorus substituents. [en ligne]. 2009. N° 26pp. 5068-5070. [Consultésans date]. DOI 10.1039/b906034k. Consulté de : ://WOS:000267500000004
[1,2,3]Triazolo[1,5-a]pyridine derivatives as molecular chemosensors for zinc(II), nitrite and cyanide anions
BALLESTEROS-GARRIDO, Rafael, ABARCA, Belen, BALLESTEROS, Rafael, RAMIREZ DE ARELLANO, Carmen, LEROUX, Frederic R., COLOBERT, Francoise et GARCIA-ESPANA, Enrique, 2009. [1,2,3]Triazolo[1,5-a]pyridine derivatives as molecular chemosensors for zinc(II), nitrite and cyanide anions. . 2009. Vol. 33, n° 10pp. 2102-2106. DOI 10.1039/b906992e.
1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study
RISTIĆ, Predrag, TODOROVIĆ, Tamara R., BLAGOJEVIĆ, Vladimir, KLISURIĆ, Olivera R., MARJANOVIĆ, Ivana, HOLLÓ, Berta Barta, VULIĆ, Predrag, GULEA, Mihaela, DONNARD, Morgan, MONGE, Miguel, RODRÍGUEZ-CASTILLO, María, LÓPEZ-DE-LUZURIAGA, José M. et FILIPOVIĆ, Nenad R., 2020. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. Crystal Growth and Design. 1 juillet 2020. DOI 10.1021/acs.cgd.0c00287. 1. .
2,2 ', 6-Tribromobiphenyl via Transition-Metal-Free ARYNE Coupling
BONNAFOUX, Laurence, COLOBERT, Francoise et LEROUX, Frederic R., 2010. 2,2 ', 6-Tribromobiphenyl via Transition-Metal-Free ARYNE Coupling: A Valuable Tool in the Synthesis of Biphenyls. [en ligne]. décembre 2010. N° 19pp. 2953-2955. [Consultésans date]. DOI 10.1055/s-0030-1259025. Consulté de : ://WOS:000284531700031 https://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0030-1259025.pdf
2,4-Bis(fluoroalkyl)quinoline-3-carboxylates as Tools for the Development of Potential Agrochemical Ingredients
ARIBI, Fallia, PANOSSIAN, Armen, VORS, J. P., PAZENOK, Sergi et LEROUX, Frederic R., 2018. 2,4-Bis(fluoroalkyl)quinoline-3-carboxylates as Tools for the Development of Potential Agrochemical Ingredients. European Journal of Organic Chemistry [en ligne]. 2018. Vol. 2018, n° 27pp. 3792-3802. [Consultésans date]. DOI 10.1002/ejoc.201800375. Consulté de : https://onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.2018003751. .
3-(Pyridin-2-yl) 1,2,3 triazolo 1,5-a quinoline
BALLESTEROS-GARRIDO, Rafael, BLANCO, Fernando, BALLESTEROS, Rafael, LEROUX, Frederic R., ABARCA, Belen, COLOBERT, Francoise, ALKORTA, Ibon et ELGUERO, Jose, 2009. 3-(Pyridin-2-yl) 1,2,3 triazolo 1,5-a quinoline: A Theoretical and Experimental Analysis of Ring-Chain Isomerisation. [en ligne]. novembre 2009. N° 33pp. 5765-5778. [Consultésans date]. DOI 10.1002/ejoc.200900818. Consulté de : ://WOS:000272330600010
3D supramolecular self-assembly of [60]fullerene hexaadducts decorated with triarylamine molecules
GAVAT, Odile, TRINH, Thi Minh Nguyet, MOULIN, Emilie, ELLIS, Thomas, MAALOUM, Mounir, BUHLER, Eric, FLEITH, Guillaume, NIERENGARTEN, Jean-François et GIUSEPPONE, Nicolas, sans date. 3D supramolecular self-assembly of [60]fullerene hexaadducts decorated with triarylamine molecules. Chemical Communications. sans date. Vol. 54, n° 55pp. 7657-7660. DOI 10.1039/C8CC04079F. 1. .
Access to Atropisomerically Enriched Biaryls by the Coupling of Aryllithiums with Arynes under Control by Homochiral Oxazolines
YALCOUYE, Boubacar, BREHIER, Anaïs, AUGROS, David, PANOSSIAN, Armen, CHOPPIN, Sabine, CHESSÉ, Matthieu, COLOBERT-LEUENBERGER, Francoise et LEROUX, Frederic R., 2016. Access to Atropisomerically Enriched Biaryls by the Coupling of Aryllithiums with Arynes under Control by Homochiral Oxazolines. European Journal of Organic Chemistry [en ligne]. 2016. Vol. 2016, n° 4pp. 725-732. [Consultésans date]. DOI 10.1002/ejoc.201501503. Consulté de : http://dx.doi.org/10.1002/ejoc.201501503
Access to heterocycles bearing emergent fluorinated substituents - as FAR as possible!
SCHMITT, Etienne, ARIBI, Fallia, PANOSSIAN, Armen, VORS, Jean-Pierre, PAZENOEK, Sergiy et LEROUX, Frederic, 2017. Access to heterocycles bearing emergent fluorinated substituents - as FAR as possible!. . 2 avril 2017. Vol. 253.
Access to the Enantiopure Axially Chiral Cyclophane Isoplagiochin D through Atropo-diastereoselective Heck Coupling
MEIDLINGER, D., MARX, L., BORDEIANU, Catalina, CHOPPIN, Sabine, COLOBERT-LEUENBERGER, Francoise et SPEICHER, A., 2018. Access to the Enantiopure Axially Chiral Cyclophane Isoplagiochin D through Atropo-diastereoselective Heck Coupling. Angewandte Chemie International Edition [en ligne]. 2018. Vol. 57, n° 29pp. 9160-9164. [Consultésans date]. DOI 10.1002/anie.201803677. Consulté de : https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.2018036771. .
Access to Wieland–Miescher Diketone-Derived Building Blocks by Stereoselective Construction of the C-9 Quaternary Carbon Center Using the Mukaiyama Aldol Reaction
SCHIAVO, Lucie, LEBEDEL, L., MASSÉ, P., CHOPPIN, Sabine et HANQUET, Gilles, 2018. Access to Wieland–Miescher Diketone-Derived Building Blocks by Stereoselective Construction of the C-9 Quaternary Carbon Center Using the Mukaiyama Aldol Reaction. The Journal of Organic Chemistry [en ligne]. 2018. Vol. 83, n° 12pp. 6247-6258. [Consultésans date]. DOI 10.1021/acs.joc.7b02862. Consulté de : https://doi.org/10.1021/acs.joc.7b028621. .
Access towards enantiopure α,α-difluoromethyl alcohols by means of sulfoxides as traceless chiral auxiliaries
BATISSE, ChloÉ, PANOSSIAN, Armen, HANQUET, Gilles et LEROUX, Frederic R., 2018. Access towards enantiopure α,α-difluoromethyl alcohols by means of sulfoxides as traceless chiral auxiliaries. Chemical Communications [en ligne]. 2018. Vol. 54, n° 74pp. 10423-10426. [Consultésans date]. DOI 10.1039/C8CC05571H. Consulté de : http://pubs.rsc.org/en/content/articlelanding/2018/cc/c8cc05571h#!divAbstract1. .
Acid-catalyzed ring-opening reactions of a cyclopropanated 3-aza-2-oxabicyclo[2.2.1]hept-5-ene with alcohols
TAIT, K., HORVATH, A., BLANCHARD, Nicolas et TAM, W., 2017. Acid-catalyzed ring-opening reactions of a cyclopropanated 3-aza-2-oxabicyclo[2.2.1]hept-5-ene with alcohols. Beilstein Journal of Organic Chemistry. 2017. Vol. 13, pp. 2888-2894. DOI 10.3762/bjoc.13.281. 1. .
Acid Fluorides in Transition-Metal Catalysis
BIZET, Vincent et BLANCHARD, Nicolas, 2019. Acid Fluorides in Transition-Metal Catalysis: A Good Balance between Stability and Reactivity. [en ligne]. 25 avril 2019. Vol. 58, pp. 6814-6817. [Consultésans date]. DOI 10.1002/anie.201900591. Consulté de : https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201900591
Acid Fluorides in Transition-Metal Catalysis: A Good Balance between Stability and Reactivity
BIZET, Vincent et BLANCHARD, Nicolas, 2019. Acid Fluorides in Transition-Metal Catalysis: A Good Balance between Stability and Reactivity. Angewandte Chemie International Edition [en ligne]. 2019. [Consultésans date]. DOI 10.1002/anie.201900591. Consulté de : https://onlinelibrary.wiley.com/doi/full/10.1002/anie.201900591
Activating pyrimidines by pre-distortion for the general synthesis of 7-aza-indazoles from 2-hydrazonylpyrimidines via intramolecular Diels-Alder reactions
LE FOULER, Vincent Le, CHEN, Yu, GANDON, Vincent, BIZET, Vincent, SALOME, Christophe, FESSARD, Thomas, LIU, Fang, HOUK, Kendall N. et BLANCHARD, Nicolas, 2019. Activating pyrimidines by pre-distortion for the general synthesis of 7-aza-indazoles from 2-hydrazonylpyrimidines via intramolecular Diels-Alder reactions. [en ligne]. 6 septembre 2019. Vol. 141, pp. 15901-15909. [Consultésans date]. DOI 10.1021/jacs.9b07037. Consulté de : https://pubs.acs.org/doi/10.1021/jacs.9b07037
Aerobic Baeyer–Villiger Oxidation Catalyzed by a Flavin-Containing Enzyme Mimic in Water
CHEVALIER, Y., KI, Y. Lock Toy, NOUEN, D. le, MAHY, J. P., GODDARD, Jean-philippe P. et AVENIER, F., 2018. Aerobic Baeyer–Villiger Oxidation Catalyzed by a Flavin-Containing Enzyme Mimic in Water. Angewandte Chemie International Edition [en ligne]. 2018. Vol. 57, n° 50pp. 16412-16415. [Consultésans date]. DOI 10.1002/anie.201810124. Consulté de : https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.2018101241. .
Allosteric inhibition of aminopeptidase N functions related to tumor growth and virus infection
SANTIAGO, C., MUDGAL, G., REGUERA, J., RECACHA, R., ALBRECHT, Sebastien, ENJUANES, L. et CASASNOVAS, J. M., 2017. Allosteric inhibition of aminopeptidase N functions related to tumor growth and virus infection. Scientific Reports [en ligne]. 2017. Vol. 7. [Consultésans date]. DOI 10.1038/srep46045. Consulté de : https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017404362&doi=10.1038%2fsrep46045&partnerID=40&md5=411bff883d90a7fc91b435829b727b021. cited By 2.
alpha-fluorinated ethers as "exotic" entity in medicinal chemistry
JESCHKE, Peter, BASTON, Eckhard et LEROUX, Frederic R., 2007. alpha-fluorinated ethers as "exotic" entity in medicinal chemistry. Mini-Reviews in Medicinal Chemistry [en ligne]. octobre 2007. Vol. 7, n° 10pp. 1027-1034. [Consultésans date]. DOI 10.2174/138955707782110150. Consulté de : ://WOS:0002498691000061. .
Aminobenzosuberone derivatives as PfA-M1 inhibitors: Molecular recognition and antiplasmodial evaluation
SALOMON, Emmanuel, SCHMITT, Marjorie, MOURAY, Elisabeth, MCEWEN, Alastair, BOUNAADJA, Lotfi, TORCHY, Morgan, POUSSIN-COURMONTAGNE, Pierre, ALAVI, Sarah, TARNUS, Celine, CAVARELLI, Jean, FLORENT, Isabelle et ALBRECHT, Sebastien, 2020. Aminobenzosuberone derivatives as PfA-M1 inhibitors: Molecular recognition and antiplasmodial evaluation. Bioorganic Chemistry [en ligne]. 1 mai 2020. Vol. 98, pp. 103750. [Consultésans date]. DOI 10.1016/j.bioorg.2020.103750. Consulté de : https://www.sciencedirect.com/science/article/abs/pii/S0045206819314026?via%3Dihub1. .

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