Laboratoire d'Innovation Moléculaire et Applications - LIMA - UMR7042

  • Flux RSS
(1 - 20 of 173)

Pages

Export to file
Bookmark
Étiquette
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.
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: 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
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. [en ligne]. octobre 2007. Vol. 7, n° 10pp. 1027-1034. [Consultésans date]. DOI 10.2174/138955707782110150. Consulté de : ://WOS:000249869100006
Aminobenzosuberone Scaffold as a Modular Chemical Tool for the Inhibition of Therapeutically Relevant M1 Aminopeptidases
SALOMON, E., SCHMITT, Marjorie, MARAPAKA, A. Kumar, STAMOGIANNOS, A., REVELANT, G., SCHMITT, C., ALAVI, Sarah, FLORENT, I., ADDLAGATTA, A., STRATIKOS, E., TARNUS, Celine et ALBRECHT, Sebastien, 2018. Aminobenzosuberone Scaffold as a Modular Chemical Tool for the Inhibition of Therapeutically Relevant M1 Aminopeptidases. Molecules [en ligne]. 2018. Vol. 23, n° 10. [Consultésans date]. DOI 10.3390/molecules23102607. Consulté de : http://www.mdpi.com/1420-3049/23/10/26071. .
Aqueous extracts of marine invertebrates from Cuba coastline display neutral aminopeptidase inhibitory activities and effects on cancer cells and Plasmodium falciparum parasites
ALONSO, I. P., BOUNAADJA, L., SÁNCHEZ, L., RIVERA, L., TARNUS, Celine, SCHMITT, Marjorie, GARCIA, G., DIAZ, L., HERNANDEZ-ZANUY, A., SÁNCHEZ, B. et FLORENT, I., 2017. Aqueous extracts of marine invertebrates from Cuba coastline display neutral aminopeptidase inhibitory activities and effects on cancer cells and Plasmodium falciparum parasites. Indian Journal of Natural Products and Resources [en ligne]. 2017. Vol. 8, n° 2pp. 107-119. [Consultésans date]. Consulté de : https://www.scopus.com/inward/record.uri?eid=2-s2.0-85026290028&partnerID=40&md5=6bcd8d6266ff31e4c39b0f78ff2c437e1. cited By 0.
Aryl transition metal chemical warheads for protein bioconjugation
BISSERET, Philippe, ABDELKAFI, H. et BLANCHARD, Nicolas, 2018. Aryl transition metal chemical warheads for protein bioconjugation. Chemical Science [en ligne]. 2018. Vol. 9, pp. 5132-5144. [Consultésans date]. DOI 10.1039/C8SC00780B. Consulté de : http://dx.doi.org/10.1039/C8SC00780B1. .
Arylmethylamino steroids as novel antiparasitic agents
KRIEG, R., JORTZIK, E., GOETZ, Alice-anne A., BLANDIN, Stephanie, WITTLIN, S., ELHABIRI, Mourad, RAHBARI, M., NURYYEVA, S., VOIGT, K., DAHSE, H. M., BRAKHAGE, A., BECKMANN, S., QUACK, T., GREVELDING, C. G., PINKERTON, A. B., SCHÖNECKER, B., BURROWS, J., DAVIOUD-CHARVET, Elisabeth, RAHLFS, S. et BECKER, K., 2017. Arylmethylamino steroids as novel antiparasitic agents. Nature Communications. 2017. Vol. 8. DOI 10.1038/ncomms14478. 1. .

Pages

Islandora displays