{"id":4938,"date":"2017-04-12T09:32:00","date_gmt":"2017-04-12T07:32:00","guid":{"rendered":"http:\/\/univet.hu\/universitaet\/mitarbeiter\/vincze-zoltan\/"},"modified":"2026-02-10T04:49:04","modified_gmt":"2026-02-10T03:49:04","slug":"vincze-zoltan","status":"publish","type":"page","link":"https:\/\/univet.hu\/de\/universitaet\/mitarbeiter\/vincze-zoltan\/","title":{"rendered":"Vincze Zolt\u00e1n"},"content":{"rendered":"<p>&nbsp;<\/p> <p>Einf\u00fchrung<\/p> <p>Im Jahr 1993 schloss ich meine Ausbildung an der Berzsenyi D\u00e1niel Grammar School in Budapest ab und wurde im Jahr 1994 an der Fakult\u00e4t f\u00fcr Naturwissenschaften der E\u00f6tv\u00f6s Lor\u00e1nd Universit\u00e4t (ELTE) zugelassen, wo ich meine Studien im Jahr 1999 abschloss und einen Abschluss als gepr\u00fcfte Chemikerin erwarb. Ich setzte meine Studien als Doktorandin mit einem Stipendium des Staates am Lehrstuhl f\u00fcr Allgemeine und Anorganische Chemie an der E\u00f6tv\u00f6s Lor\u00e1nd Universit\u00e4t fort, unter der Betreuung von Dr. Andr\u00e1s Kotschy. Im Jahr 2006 erlangte ich meinen Doktortitel mit der Auszeichnung summa cum laude. Der Titel meiner Dissertation lautete &#8222;Anwendung moderner Methoden bei der Synthese heterocyclischer Verbindungen.&#8220;<\/p> <p>Seit 2001 habe ich in verschiedenen Positionen an der Universit\u00e4t f\u00fcr Veterin\u00e4rmedizin Budapest gearbeitet.<\/p> <p>Hauptforschungsbereiche:<\/p> <p>Synthese von biologisch aktiven heterocyclischen Verbindungen, einschlie\u00dflich der Herstellung von Wirkstoffen gegen Biofilme und Derivaten von Sulfid-Donatoren.<\/p> <p>Ver\u00f6ffentlichungen<\/p> <p>MTMT:<\/p> <table class=\"table table-striped\" width=\"972\"> <tbody> <tr> <td>1.<\/td> <td><span data-contrast=\"auto\">Z. Vincze, A.\u00a0B.B\u00edr\u00f3, M.\u00a0Cs\u00e9kei, G. Tim\u00e1ri, A.\u00a0Kotschy\u00a0(2006) The\u00a0palladium\u00a0catalyzed\u00a0preparation of\u00a0condensed\u00a0tetracyclic\u00a0heterocycles\u00a0and\u00a0its\u00a0application\u00a0to\u00a0the\u00a0synthesis\u00a0of\u00a0<\/span><i><span data-contrast=\"auto\">rac<\/span><\/i><span data-contrast=\"auto\">-mangochinine.\u00a0<\/span><i><span data-contrast=\"auto\">Synthesis<\/span><\/i><span data-contrast=\"auto\">, 1375-1385.<\/span>\u00a0<span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:6,&quot;335551620&quot;:6,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><\/td> <\/tr> <tr> <td>2.<\/td> <td> <p><span data-contrast=\"auto\">Z. Nov\u00e1k, Z. Vincze,\u00a0Zs.\u00a0Cz\u00e9g\u00e9ny, G.\u00a0Magyarfalvi, D. M. Smith, A.\u00a0Kotschy\u00a0(2006)\u00a0Study\u00a0of\u00a0the\u00a0formation\u00a0and\u00a0thermal\u00a0decomposition\u00a0of an\u00a0azo-bridged\u00a0tricyclic\u00a0ring\u00a0system.<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559739&quot;:160,&quot;335559740&quot;:240}\">\u00a0<\/span><\/p> <p><i><span data-contrast=\"auto\">Eur. J.\u00a0Org.\u00a0Chem.,<\/span><\/i><span data-contrast=\"auto\">\u00a0<\/span><b><span data-contrast=\"auto\">15<\/span><\/b><span data-contrast=\"auto\">, 3358-3363.\u00a0<\/span>\u00a0<span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559685&quot;:708,&quot;335559739&quot;:160,&quot;335559740&quot;:259}\">\u00a0<\/span><\/td> <\/tr> <tr> <td>3.<\/td> <td><span data-contrast=\"auto\">Vincze, Z. Mucs<\/span><span data-contrast=\"auto\">Z<\/span><span data-contrast=\"auto\">i, P. Scheiber, P. Nemes (2008)<\/span><span data-contrast=\"auto\">1,6-Electrocyclisation of 1-Azatriene Derivatives.\u00a0<\/span><i><span data-contrast=\"auto\">Eur. J.\u00a0Org.\u00a0Chem.,<\/span><\/i><span data-contrast=\"auto\">\u00a0<\/span><b><span data-contrast=\"auto\">6<\/span><\/b><span data-contrast=\"auto\">, 1092-1100.<\/span><\/td> <\/tr> <tr> <td>4.<\/td> <td>G. Maksay,\u00a0P.Nemes, Z. Vincze T.\u00a0B\u00edr\u00f3\u00a0(2008)\u00a0Synthesis\u00a0of (nor)tropeine\u00a0(di)esters\u00a0and\u00a0allosteric\u00a0modulation\u00a0of\u00a0glycine\u00a0receptor\u00a0binding.\u00a0Bioorg\u00a0Med Chem.,\u00a016, 2086-2092.<span data-contrast=\"auto\">\u00a0<\/span>\u00a0<span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559685&quot;:708,&quot;335559739&quot;:160,&quot;335559740&quot;:259,&quot;335559991&quot;:345,&quot;469777462&quot;:[360],&quot;469777927&quot;:[0],&quot;469777928&quot;:[1]}\">\u00a0<\/span><\/td> <\/tr> <tr> <td>5.<\/td> <td><span data-contrast=\"auto\">G. Maksay, Z. Vincze, P. Nemes<\/span><span data-contrast=\"auto\">\u00a0(2009)\u00a0<\/span><a href=\"http:\/\/apps.wosportal.om.hu\/full_record.do?product=WOS&amp;search_mode=GeneralSearch&amp;qid=1&amp;SID=W1AHfbbnho4H7Da45H3&amp;page=1&amp;doc=1\"><span data-contrast=\"auto\">Synthesis of heteroaromatic tropeines and heterogeneous binding to glycine receptors<\/span><\/a><span data-contrast=\"auto\">.\u00a0<\/span><i><span data-contrast=\"auto\">Bioorg\u00a0Med Chem<\/span><\/i><span data-contrast=\"auto\">.\u00a0<\/span><b><span data-contrast=\"auto\">17<\/span><\/b><span data-contrast=\"auto\">, 6872-6878.\u00a0<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559685&quot;:708,&quot;335559739&quot;:160,&quot;335559740&quot;:259,&quot;335559991&quot;:345,&quot;469777462&quot;:[360],&quot;469777927&quot;:[0],&quot;469777928&quot;:[1]}\">\u00a0<\/span><\/td> <\/tr> <tr> <td>6.<\/td> <td><span data-contrast=\"auto\">Vincze Zolt\u00e1n, Nemes P\u00e9ter (2011)\u00a0Synthesis\u00a0and\u00a0cyclizations\u00a0of 1-azapolyene\u00a0derivatives.\u00a0\u00a0<\/span><i><span data-contrast=\"auto\">Tetrahedron<\/span><\/i><span data-contrast=\"auto\">,\u00a0\u00a0<\/span><b><span data-contrast=\"auto\">67<\/span><\/b><span data-contrast=\"auto\">, 3380-3387.\u00a0<\/span><\/td> <\/tr> <tr> <td>7.<\/td> <td><span data-contrast=\"auto\">Vincze Zolt\u00e1n, Nemes P\u00e9ter (2013) A\u00a0novel\u00a0strategy\u00a0for\u00a0the\u00a0synthesis\u00a0of 2,6-diaryl-1,2-dihydropyridines\u00a0via\u00a06p-electrocyclization\u00a0Tetrahedron\u00a0<\/span><b><span data-contrast=\"auto\">69<\/span><\/b><span data-contrast=\"auto\">\u00a06269-6274.<\/span><\/td> <\/tr> <tr> <td>8.<\/td> <td>M<span data-contrast=\"auto\">ih\u00e1ly V\u00a0Pilipecz, P\u00e1l Scheiber, Zolt\u00e1n Vincze, Tam\u00e1s R Varga, G\u00e1bor T\u00f3th, P\u00e9ter Nemes (2014)\u00a0One-pot\u00a0reactions\u00a0of\u00a0nitroenamines\u00a0with\u00a0anilines and\u00a0ethyl\u00a0glyoxylate\u00a0<\/span><i><span data-contrast=\"auto\">Tetrahedron<\/span><\/i><span data-contrast=\"auto\">\u00a0<\/span><b><span data-contrast=\"auto\">70\u00a0<\/span><\/b><span data-contrast=\"auto\">4355-4360.<\/span><\/td> <\/tr> <tr> <td>9.<\/td> <td><span data-contrast=\"auto\">\u00a0<\/span><span data-contrast=\"none\">Aradi,\u00a0K ;\u00a0Meszaros,\u00a0A ;\u00a0Toth,\u00a0BL ;\u00a0Vincze,\u00a0Z ;\u00a0Novak,\u00a0Z<\/span><span data-contrast=\"auto\">\u00a0,\u00a0<\/span><span data-contrast=\"none\">Copper-Catalyzed\u00a0N-Arylation\u00a0of\u00a0Nitroenamines\u00a0with\u00a0Diaryliodonium\u00a0Salts\u00a0<\/span><span data-contrast=\"auto\">JOURNAL OF ORGANIC CHEMISTRY\u00a082 :\u00a022 pp. 11752-11764. ,\u00a013 p. (2017)\u00a0<\/span><span data-ccp-props=\"{&quot;134233117&quot;:true,&quot;134233118&quot;:true,&quot;201341983&quot;:0,&quot;335559685&quot;:600,&quot;335559739&quot;:160,&quot;335559740&quot;:259,&quot;335559991&quot;:174}\">\u00a0<\/span><\/td> <\/tr> <tr> <td>10.<\/td> <td><span data-contrast=\"none\">Pilipecz,\u00a0Mihaly\u00a0V\u00a0;\u00a0Varga,\u00a0Tamas\u00a0R.\u00a0;\u00a0Krall,\u00a0Peter\u00a0;\u00a0Vincze,\u00a0Zoltan\u00a0;\u00a0Mucsi,\u00a0Zoltan\u00a0;\u00a0Deme,\u00a0Ruth\u00a0;\u00a0Szabo,\u00a0Pal\u00a0T.\u00a0;\u00a0Nemes, Peter\u00a0Simple\u00a0route\u00a0to\u00a0new\u00a0oxadiazaboroles\u00a0and\u00a0oxadiazoles\u00a0via\u00a0amidoximes\u00a0<\/span><span data-contrast=\"auto\">SYNTHETIC COMMUNICATIONS\u00a0<\/span><b><span data-contrast=\"auto\">50<\/span><\/b><span data-contrast=\"auto\">\u00a0:\u00a011 pp. 1712-1723. ,\u00a012 p. (2020)\u00a0<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559685&quot;:709,&quot;335559739&quot;:160,&quot;335559740&quot;:259,&quot;335559991&quot;:283}\">\u00a0<\/span><\/td> <\/tr> <\/tbody> <\/table> <p>&nbsp;<\/p>","protected":false},"excerpt":{"rendered":"<p>&nbsp; Einf\u00fchrung Im Jahr 1993 schloss ich meine Ausbildung an der Berzsenyi D\u00e1niel Grammar School in Budapest ab und wurde im Jahr 1994 an der Fakult\u00e4t f\u00fcr Naturwissenschaften der E\u00f6tv\u00f6s Lor\u00e1nd Universit\u00e4t (ELTE) zugelassen, wo ich meine Studien im Jahr 1999 abschloss und einen Abschluss als gepr\u00fcfte Chemikerin erwarb. Ich setzte meine Studien als Doktorandin<\/p>\n","protected":false},"author":5824,"featured_media":0,"parent":859,"menu_order":211,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"categories":[55],"tags":[],"class_list":["post-4938","page","type-page","status-publish","hentry","category-mitarbeiter"],"acf":[],"_links":{"self":[{"href":"https:\/\/univet.hu\/de\/wp-json\/wp\/v2\/pages\/4938","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/univet.hu\/de\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/univet.hu\/de\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/univet.hu\/de\/wp-json\/wp\/v2\/users\/5824"}],"replies":[{"embeddable":true,"href":"https:\/\/univet.hu\/de\/wp-json\/wp\/v2\/comments?post=4938"}],"version-history":[{"count":1,"href":"https:\/\/univet.hu\/de\/wp-json\/wp\/v2\/pages\/4938\/revisions"}],"predecessor-version":[{"id":200908,"href":"https:\/\/univet.hu\/de\/wp-json\/wp\/v2\/pages\/4938\/revisions\/200908"}],"up":[{"embeddable":true,"href":"https:\/\/univet.hu\/de\/wp-json\/wp\/v2\/pages\/859"}],"wp:attachment":[{"href":"https:\/\/univet.hu\/de\/wp-json\/wp\/v2\/media?parent=4938"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/univet.hu\/de\/wp-json\/wp\/v2\/categories?post=4938"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/univet.hu\/de\/wp-json\/wp\/v2\/tags?post=4938"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}