Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Claude Commandeur"'
Autor:
Charles-Henry Fabritius, Paulina Węgrzyn, Agata Stasiowska, Marta Bugaj, Andrzej Mazan, Monika Dobrzańska, Karolina Gluza, Piotr Kowalczyk, Ewa Kolasińska, Adrian Zarebski, Przemyslaw Zawadzki, Karolina Krawczynska, Aneta Bobowska, Anna Cierpich, Małgorzata Żurawska, Nicolas Boutard, Mariusz Milik, Katarzyna Wiklik, Anna Buda, Małgorzata Jarosz, Krzysztof Brzózka, Aleksandra Sabiniarz, Mariusz Galek, Edyta Palacz, Klaudia Czerwińska, Claude Commandeur
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 29:607-613
Maternal embryonic leucine zipper kinase (MELK) is involved in several key cellular processes and displays increased levels of expression in numerous cancer classes (colon, breast, brain, ovary, prostate and lung). Although no selective MELK inhibito
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0811d2cb5e37f7797b44a0953a2ff63
https://doi.org/10.1016/j.bmcl.2018.12.051
https://doi.org/10.1016/j.bmcl.2018.12.051
Publikováno v:
Pure and Applied Chemistry. 84:1567-1574
An advanced spiroketal intermediate toward the synthesis of 39-oxobistramide K was prepared, fragment C14–C40. This fragment was obtained in 19 steps with an overall yield of 6.2 % using a FeCl3-catalyzed spiroketalization as the key step.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38c639e0a05583605f1fafbdd434696e
https://doi.org/10.1351/pac-con-11-09-06
https://doi.org/10.1351/pac-con-11-09-06
Autor:
Malgorzata Commandeur, Léon Ghosez, Andrew Edmunds, Peter Maienfisch, Claude Commandeur, Brice Kauffmann, Kathell Bathany
Publikováno v:
Tetrahedron. 67:9899-9908
This report describes a detailed study of the oxidation-Meisenheimer rearrangement of N-methyl-3-hydroxy-7-chloropyrroloindoline ethyl ester and the corresponding O-Boc and N-Boc derivatives. Experimental conditions were found, which allowed the sele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc5d3fbce3f6d54247d57c9648820cdf
https://doi.org/10.1016/j.tet.2011.09.112
https://doi.org/10.1016/j.tet.2011.09.112
Publikováno v:
European Journal of Organic Chemistry. 2011:1447-1451
Figure 1. Examples of pyranoacridines.[a] CNRS UMR 176,26 Rue d’Ulm, 75248 Paris, FranceFax: +33-1-56-24-66-31E-mail: claude.commandeur@curie.fremmanuel.bertounesque@curie.fr[b] Institut Curie, Centre de Recherche,26 Rue d’Ulm, 75248 Paris, Franc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5c4da4a3735b1f718016b177feaf818
https://doi.org/10.1002/ejoc.201001598
https://doi.org/10.1002/ejoc.201001598
Autor:
Claude Commandeur, Peter Maienfisch, Léon Ghosez, Andrew Edmunds, Malgorzata Commandeur, Michaël De Paolis
Publikováno v:
Tetrahedron Letters. 50:3359-3362
A highly effective procedure is reported to synthesize a substituted bicyclo[4.2.0]octenol derivative by regioselective cycloaddition of phenyl-1-propynyl sulfide with cyclohexenone followed by selective reduction of the ketone group and reductive el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6570df5cbf92f4572364fa528b4bffc8
https://doi.org/10.1016/j.tetlet.2009.02.105
https://doi.org/10.1016/j.tetlet.2009.02.105
Publikováno v:
European Journal of Organic Chemistry. 2007:3045-3052
In order to obtain functionalized naphthoquinones, a systematic study of the Kochi–Anderson procedure for the alkylation of quinones is presented. While linear amino acids of different lengths were good substrates for this decarboxylation procedure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63562711c2e56aea6e559e42461021ea
https://doi.org/10.1002/ejoc.200700135
https://doi.org/10.1002/ejoc.200700135
Autor:
Amandine Guérinot, Anna Serra-Muns, Johan Cornil, Charlelie Bensoussan, Claude Commandeur, Janine Cossy, Christian Gnamm, Sébastien Reymond, Malgorzata Commandeur, Laurine Gonnard
Publikováno v:
ChemInform. 46
ConspectusA myriad of natural and/or biologically active products include nitrogen- and oxygen-containing saturated heterocycles, which are thus considered as attractive scaffolds in the drug discovery process. As a consequence, a wide range of react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48871f3f3dda87edb6a20c9adb590e27
https://doi.org/10.1002/chin.201521297
https://doi.org/10.1002/chin.201521297
Autor:
Sébastien Reymond, Laurine Gonnard, Claude Commandeur, Amandine Guérinot, Anna Serra-Muns, Malgorzata Commandeur, Charlelie Bensoussan, Christian Gnamm, Janine Cossy, Johan Cornil
Publikováno v:
Accounts of chemical research. 48(3)
A myriad of natural and/or biologically active products include nitrogen- and oxygen-containing saturated heterocycles, which are thus considered as attractive scaffolds in the drug discovery process. As a consequence, a wide range of reactions has b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3eb1d3840f199d45cdff4ae107e5c1bc
https://pubmed.ncbi.nlm.nih.gov/25674664
https://pubmed.ncbi.nlm.nih.gov/25674664
Autor:
Max Malacria, Marcial Moreno-Mañas, Vicenç Branchadell, Claude Commandeur, Roser Pleixats, Cecile Boglio, Serge Thorimbert
Publikováno v:
Journal of Organometallic Chemistry. 687:337-345
Regioselectivity of the Tsuji-Trost reaction on allyl acetates and carbonates substituted with silyl groups at the olefinic moiety has been analyzed. Silicon atom in the central carbon atom increases the stability of the intermediate π-allylpalladiu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56e9caa790440f08146b94011047eca6
https://doi.org/10.1016/s0022-328x(03)00664-8
https://doi.org/10.1016/s0022-328x(03)00664-8
Autor:
Serge Thorimbert, Maxime R. Vitale, Max Malacria, Giovanni Poli, Giuliano Giambastiani, Claude Commandeur
Publikováno v:
Scopus-Elsevier
European journal of organic chemistry
(2003): 2702–2708. doi:10.1002/ejoc.200300086
info:cnr-pdr/source/autori:Serge, Thorimbert; Giuliano, Giambastiani; Claude, Commandeur; Maxime, Vitale; Giovanni, Poli; Max, Malacria/titolo:Diastereoselective Preparation of Silylated Pyrrolidones via Palladium-Catalysed Cyclizations/doi:10.1002%2Fejoc.200300086/rivista:European journal of organic chemistry (Print)/anno:2003/pagina_da:2702/pagina_a:2708/intervallo_pagine:2702–2708/volume
European journal of organic chemistry
(2003): 2702–2708. doi:10.1002/ejoc.200300086
info:cnr-pdr/source/autori:Serge, Thorimbert; Giuliano, Giambastiani; Claude, Commandeur; Maxime, Vitale; Giovanni, Poli; Max, Malacria/titolo:Diastereoselective Preparation of Silylated Pyrrolidones via Palladium-Catalysed Cyclizations/doi:10.1002%2Fejoc.200300086/rivista:European journal of organic chemistry (Print)/anno:2003/pagina_da:2702/pagina_a:2708/intervallo_pagine:2702–2708/volume
A new palladium-catalysed allylic alkylation affording silylated 3-vinylpyrrolidones has been developed. The method relies upon the interaction between a stabilized acetamide enolate anion and a silicon-containing, nitrogen-tethered η3-allylpalladiu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b946a46634a43f3d96125ece431e864b
https://doi.org/10.1002/ejoc.200300086
https://doi.org/10.1002/ejoc.200300086