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<SDOBI lang="fr"><B000><eptags><B001EP>ATBECHDEDKESFRGBGRITLILUNLSEMCPTIESILTLVFIROMKCYALTRBGCZEEHUPLSK..HRIS..MTNORS..SM..................</B001EP><B003EP>*</B003EP><B005EP>J</B005EP><B007EP>BDM Ver 0.1.63 (23 May 2017) -  2999001/0</B007EP></eptags></B000><B100><B110>2542532</B110><B120><B121>FASCICULE DE BREVET EUROPEEN CORRIGE</B121></B120><B130>B8</B130><B132EP>B1</B132EP><B140><date>20180214</date></B140><B150><B151>W1</B151><B153>74</B153><B155><B1551>de</B1551><B1552>Bibliographie</B1552><B1551>en</B1551><B1552>Bibliography</B1552><B1551>fr</B1551><B1552>Bibliographie</B1552></B155></B150><B190>EP</B190></B100><B200><B210>11700249.3</B210><B220><date>20110107</date></B220><B240><B241><date>20121102</date></B241><B242><date>20130806</date></B242></B240><B250>fr</B250><B251EP>fr</B251EP><B260>fr</B260></B200><B300><B310>1050108</B310><B320><date>20100108</date></B320><B330><ctry>FR</ctry></B330></B300><B400><B405><date>20180214</date><bnum>201807</bnum></B405><B430><date>20130109</date><bnum>201302</bnum></B430><B450><date>20180103</date><bnum>201801</bnum></B450><B452EP><date>20170905</date></B452EP><B480><date>20180214</date><bnum>201807</bnum></B480></B400><B500><B510EP><classification-ipcr sequence="1"><text>C07D 233/58        20060101AFI20110728BHEP        </text></classification-ipcr><classification-ipcr sequence="2"><text>C07F  15/00        20060101ALI20110728BHEP        </text></classification-ipcr><classification-ipcr sequence="3"><text>C08G  77/08        20060101ALI20110728BHEP        </text></classification-ipcr></B510EP><B540><B541>de</B541><B542>VERFAHREN ZUR HERSTELLUNG VON CARBEN IN EINER LÖSUNG UND STABILE FORM VOM DURCH DIESES VERFAHREN HERGESTELLTEN CARBEN</B542><B541>en</B541><B542>METHOD FOR PREPARING CARBENE IN SOLUTION AND STABLE FORM OF CARBENE OBTAINED BY SAID METHOD</B542><B541>fr</B541><B542>PROCÉDÉ DE PRÉPARATION DE CARBÈNE EN SOLUTION ET FORME STABLE DE CARBÈNE OBTENU PAR CE PROCÉDÉ</B542></B540><B560><B562><text>KNISHEVITSKY A V ET AL: "Copper(I) halide complexes of the new 4,4'-bridged heteroaromatic biscarbenes of the 1,2,4-triazole series", JOURNAL OF ORGANOMETALLIC CHEMISTRY, ELSEVIER-SEQUOIA S.A. LAUSANNE, CH, vol. 693, no. 8-9, 15 avril 2008 (2008-04-15), pages 1405-1411, XP022590097, ISSN: 0022-328X, DOI: DOI:10.1016/J.JORGANCHEM.2007.07.056 [extrait le 2008-04-05]</text></B562><B562><text>CHEN HAO ET AL: "Proton affinities of N-heterocyclic carbene super bases.", ORGANIC LETTERS 1 SEP 2005 LNKD- PUBMED:16119939, vol. 7, no. 18, 1 septembre 2005 (2005-09-01), pages 3949-3952, XP002627477, ISSN: 1523-7060</text></B562><B562><text>SCHOLL M ET AL: "SYNTHESIS AND ACTIVITY OF A NEW GENERATION OF RUTHENIUM-BASED OLEFIN METATHESIS CATALYSTS COORDINATED WITH 1,3-DIMESITYL-4,5-DIHYDROIMIDAZ OL-2-YLIDENE LIGANDS", ORGANIC LETTERS, AMERICAN CHEMICAL SOCIETY, US, vol. 1, no. 6, 1 janvier 1999 (1999-01-01) , pages 953-956, XP000984756, ISSN: 1523-7060, DOI: DOI:10.1021/OL990909Q</text></B562><B562><text>TINA M TRNKA ET AL: "Synthesis and Activity of Ruthenium Alkylidene Complexes Coordinated with Phosphine and N-Heterocyclic Carbene Ligands", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, AMERICAN CHEMICAL SOCIETY, US, vol. 125, no. 9, 1 juillet 2003 (2003-07-01), pages 2546-2558, XP001537178, ISSN: 0002-7863, DOI: DOI:10.1021/JA021146W [extrait le 2003-02-12]</text></B562><B562><text>Nikolai I. Korotkikh ET AL: "Tandem transformations of 1,2,4-triazol-5-ylidenes into 5-amidino-1,2,4-triazoles", ARKIVOC, 1 January 2007 (2007-01-01), pages 156-172, XP055073628, Retrieved from the Internet: URL:http://www.arkat-usa.org/get-file/2327 9/ [retrieved on 2013-07-31]</text></B562><B562><text>Mohammad Movassaghi ET AL: "N-Heterocyclic Carbene-Catalyzed Amidation of Unactivated Esters with Amino Alcohols", Organic Letters, vol. 7, no. 12, 1 June 2005 (2005-06-01), pages 2453-2456, XP055018304, ISSN: 1523-7060, DOI: 10.1021/ol050773y</text></B562><B562><text>Olivier Coulembier ET AL: "Alcohol Adducts of N -Heterocyclic Carbenes:  Latent Catalysts for the Thermally-Controlled Living Polymerization of Cyclic Esters", Macromolecules, vol. 39, no. 17, 1 August 2006 (2006-08-01), pages 5617-5628, XP055065316, ISSN: 0024-9297, DOI: 10.1021/ma0611366</text></B562></B560></B500><B700><B720><B721><snm>MALIVERNEY, Christian</snm><adr><str>La Bigaudière</str><city>F-69690 Saint Julien Sur Bibost</city><ctry>FR</ctry></adr></B721><B721><snm>SAINT-JALMES, Laurent</snm><adr><str>46 rue Charles de Gaulle</str><city>F-69390 Vourles</city><ctry>FR</ctry></adr></B721><B721><snm>BACEIREDO, Antoine, J.</snm><adr><str>2 rue Raymond Boulogne, Apt D41</str><city>31500 Toulouse</city><ctry>FR</ctry></adr></B721><B721><snm>KATO, Tsuyoshi</snm><adr><str>19, rue de Nîmes, Bât. B, Apt. 13</str><city>31400 Toulouse</city><ctry>FR</ctry></adr></B721><B721><snm>GOJON, Sophie</snm><adr><str>4 avenue Alsace Lorraine</str><city>92500 Rueil-Malmaison</city><ctry>FR</ctry></adr></B721></B720><B730><B731><snm>Bluestar Silicones France SAS</snm><iid>101085793</iid><irf>DO 10001</irf><adr><str>21 Avenue Georges Pompidou</str><city>69003 Lyon</city><ctry>FR</ctry></adr></B731><B731><snm>CNRS</snm><iid>101080651</iid><irf>DO 10001</irf><adr><str>3 Rue Michel Ange</str><city>75016 Paris</city><ctry>FR</ctry></adr></B731></B730><B740><B741><snm>Mekki, Boualem</snm><iid>101118677</iid><adr><str>Bluestar Silicones France 
Dépt. Brevets - Bât. 77 
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