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Mathematisch-Naturwissenschaftliche Fakultät</field><field name="allMeta">Mathematisch-Natur-&lt;br /&gt;wissenschaftliche Fakultät</field><field name="allMeta">Uni.Rostock.Fakultaet.MNF</field><field name="allMeta">http://d-nb.info/gnd/2147083-2</field><field name="category">licenseinfo:work</field><field name="category.top">licenseinfo:work</field><field name="allMeta">Werk</field><field name="allMeta">work</field><field name="category">licenseinfo:work.rightsreserved</field><field name="category.top">licenseinfo:work.rightsreserved</field><field name="allMeta">alle Rechte vorbehalten</field><field name="allMeta">all rights reserved</field><field name="allMeta">/creativecommons/r/reserved/0.9/88x31.png</field><field name="allMeta">[DE-28]Urheberrechtsschutz 1.0$gRights Statements$uhttp://rightsstatements.org/vocab/InC/1.0/</field><field name="allMeta">http://rightsstatements.org/vocab/InC/1.0/</field><field name="allMeta">http://rightsstatements.org/vocab/InC/1.0/</field><field name="category">licenseinfo:deposit</field><field name="category.top">licenseinfo:deposit</field><field name="allMeta">Veröffentlichungsgenehmigung</field><field name="allMeta">permission to store</field><field name="category">licenseinfo:deposit.rightsgranted</field><field name="category.top">licenseinfo:deposit.rightsgranted</field><field name="allMeta">Nutzungsrechte erteilt</field><field name="allMeta">rights granted</field><field name="category">licenseinfo:metadata</field><field name="category.top">licenseinfo:metadata</field><field name="allMeta">Lizenzen für Metadaten</field><field name="category">licenseinfo:metadata.cc0</field><field name="category.top">licenseinfo:metadata.cc0</field><field name="allMeta">Lizenz Metadaten: CC0</field><field name="allMeta">license metadata: CC0</field><field name="allMeta">/creativecommons/p/zero/1.0/88x31.png</field><field name="allMeta">https://creativecommons.org/publicdomain/zero/1.0/</field><field name="category">accesscondition:openaccess</field><field name="category.top">accesscondition:openaccess</field><field name="allMeta">frei zugänglich (Open Access)</field><field name="allMeta">open access</field><field name="allMeta">http://purl.org/coar/access_right/c_abf2</field><field name="allMeta">OA</field><field name="allMeta">free</field><field name="allMeta">info:eu-repo/semantics/openAccess</field><field name="allMeta">[DE-28]Open Access$gControlled Vocabulary for Access Rights$uhttp://purl.org/coar/access_right/c_abf2</field><field name="category">rfc5646:en</field><field name="category.top">rfc5646:en</field><field name="allMeta">Englisch</field><field name="allMeta">English</field><field name="allMeta">eng</field><field name="allMeta">eng</field><field name="mods.title">Synthesis of novel quinolines, pyrrolo[2,3-b]indoles, and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactions</field><field name="mods.title.main">Synthesis of novel quinolines, pyrrolo[2,3-b]indoles, and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactions</field><field name="mods.title.subtitle"></field><field name="mods.nameIdentifier">gnd:1154322130</field><field name="mods.nameIdentifier">gnd:132314614</field><field name="mods.nameIdentifier">gnd:11370979X</field><field name="mods.nameIdentifier">orcid:0000-0001-9809-724X</field><field name="mods.nameIdentifier">gnd:38329-6</field><field name="mods.nameIdentifier">gnd:2147083-2</field><field name="mods.nameIdentifier.top">gnd:1154322130</field><field name="mods.nameIdentifier.top">gnd:132314614</field><field name="mods.nameIdentifier.top">gnd:11370979X</field><field name="mods.nameIdentifier.top">orcid:0000-0001-9809-724X</field><field name="mods.nameIdentifier.top">gnd:38329-6</field><field name="mods.nameIdentifier.top">gnd:2147083-2</field><doc><field name="id">rosdok_disshab_0000002064-d36530e54</field><field name="mods.nameIdentifier">gnd:1154322130</field><field name="mods.name">Maksym Cherevatenko</field><field name="mods.name.top">Maksym Cherevatenko</field></doc><doc><field name="id">rosdok_disshab_0000002064-d36530e68</field><field name="mods.nameIdentifier">gnd:132314614</field><field name="mods.name">Peter Langer</field><field name="mods.name.top">Peter Langer</field></doc><doc><field name="id">rosdok_disshab_0000002064-d36530e82</field><field name="mods.nameIdentifier">gnd:11370979X</field><field name="mods.nameIdentifier">orcid:0000-0001-9809-724X</field><field name="mods.name">Thomas J. J. Müller</field><field name="mods.name.top">Thomas J. J. Müller</field></doc><doc><field name="id">rosdok_disshab_0000002064-d36530e97</field><field name="mods.nameIdentifier">gnd:38329-6</field><field name="mods.name">Universität Rostock</field><field name="mods.name.top">Universität Rostock</field></doc><doc><field name="id">rosdok_disshab_0000002064-d36530e108</field><field name="mods.nameIdentifier">gnd:2147083-2</field><field name="mods.name">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.name.top">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field></doc><field name="mods.name">Maksym Cherevatenko</field><field name="mods.name">Peter Langer</field><field name="mods.name">Thomas J. J. Müller</field><field name="mods.name">Universität Rostock</field><field name="mods.name">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.name.top">Maksym Cherevatenko</field><field name="mods.name.top">Peter Langer</field><field name="mods.name.top">Thomas J. J. Müller</field><field name="mods.name.top">Universität Rostock</field><field name="mods.name.top">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.author">Maksym Cherevatenko</field><field name="mods.place">Rostock</field><field name="mods.publisher">Universität Rostock</field><field name="mods.genre">epub.dissertation</field><field name="mods.identifier">http://purl.uni-rostock.de/rosdok/id00002414</field><field name="mods.identifier">urn:nbn:de:gbv:28-rosdok_id00002414-0</field><field name="mods.identifier">10.18453/rosdok_id00002414</field><field name="mods.subject">Chinolin</field><field name="mods.subject">Arylierung</field><field name="mods.abstract">The present thesis is mainly dedicated to the study of the synthesis of quinolines, pyrolo[2,3-b]indoles and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactions. This includes arylation of quinolines via Suzuki-Miyaura and alkynylation of 4-trifluoromethylquinolines via Sonogashira reaction. Consequent synthesis of a wide range of fused pyridines and their further modifications were successfully performed. A number of pyrolo[2,3-b]indoles and pyrimido[4,5-b]indole-2,4(3H,9H)-diones were synthesized with the usage of Buchwald-Hartwig reaction.</field><field name="mods.abstract">Die vorliegende Arbeit beschäftigt sich mit der Synthese von Chinolinen, Pyrolo[2,3-b]indolen und 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-dionen durch Palladium-katalysierte Kreuzkupplungsreaktionen. Sie beinhaltet Arylierungen von Chinolinen mittels Suzuki-Miyaura-Reaktion und Alkinylierung von 4-Trifluoromethylchinolinen mittels Sonogashira-Reaktion. Außerdem wurden verschiedene Pyrolo[2,3-b]indole und Pyrimido[4,5-b]indole-2,4(3H,9H)-dione durch Buchwald-Hartwig-Reaktion hergestellt.</field><field name="mods.dateIssued">2017</field><field name="mods.yearIssued">2017</field><field name="mods.note.statement of responsibility">vorgelegt von M. Sc. Maksym Cherevatenko</field><field name="mods.type">epub.dissertation</field><field name="search_result_link_text">1
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        rosdok/id000024141049230329Oau2019-02-152023-08-05T19:12:04ZrdaConverted from PICA to MODS using Pica2Mods XSLT Transformer 2.7 [SCM: "0c0e7a3c226a4a0cbcbec39b493c3c5257339ab8" "v2.7" "2023-08-04T00:00:00+0200"] with mode 'DEFAULT'.DissertationHochschulschriftSynthesis of novel quinolines, pyrrolo[2,3-b]indoles, and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactionsThe present thesis is mainly dedicated to the study of the synthesis of quinolines, pyrolo[2,3-b]indoles and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactions. This includes arylation of quinolines via Suzuki-Miyaura and alkynylation of 4-trifluoromethylquinolines via Sonogashira reaction. Consequent synthesis of a wide range of fused pyridines and their further modifications were successfully performed. A number of pyrolo[2,3-b]indoles and pyrimido[4,5-b]indole-2,4(3H,9H)-diones were synthesized with the usage of Buchwald-Hartwig reaction.Die vorliegende Arbeit beschäftigt sich mit der Synthese von Chinolinen, Pyrolo[2,3-b]indolen und 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-dionen durch Palladium-katalysierte Kreuzkupplungsreaktionen. Sie beinhaltet Arylierungen von Chinolinen mittels Suzuki-Miyaura-Reaktion und Alkinylierung von 4-Trifluoromethylchinolinen mittels Sonogashira-Reaktion. Außerdem wurden verschiedene Pyrolo[2,3-b]indole und Pyrimido[4,5-b]indole-2,4(3H,9H)-dione durch Buchwald-Hartwig-Reaktion hergestellt.MaksymCherevatenko1988 -VerfasserInaut1154322130PeterLanger1969 -AkademischeR BetreuerIndgs132314614Thomas J. J.MüllerAkademischeR BetreuerIndgs11370979X0000-0001-9809-724X38329-6Universität Rostock1419 -Grad-verleihende Institutiondgg2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgghttp://purl.uni-rostock.de/rosdok/id00002414urn:nbn:de:gbv:28-rosdok_id00002414-010.18453/rosdok_id00002414540 ChemieMathematisch-Naturwissenschaftliche Fakultätalle Rechte vorbehaltenNutzungsrechte erteiltLizenz Metadaten: CC0frei zugänglich (Open Access)en2017Universität RostockRostockmonographic201720172019Universitätsbibliothek RostockRostock2019Universitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00002414vorgelegt von M. Sc. Maksym CherevatenkoChinolinArylierung
      
    
  
  
    
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      administrator</field><field name="derivateLabel">fulltext</field><field name="ir.pdffulltext_url">file/rosdok_disshab_0000002064/rosdok_derivate_0000066142/Cherevatenko_Dissertation_2019.pdf</field><field name="mods.title">Synthesis of novel quinolines, pyrrolo[2,3-b]indoles, and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactions</field><field name="mods.title.main">Synthesis of novel quinolines, pyrrolo[2,3-b]indoles, and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactions</field><field name="mods.title.subtitle"></field><field name="mods.nameIdentifier">gnd:1154322130</field><field name="mods.nameIdentifier">gnd:132314614</field><field name="mods.nameIdentifier">gnd:11370979X</field><field name="mods.nameIdentifier">orcid:0000-0001-9809-724X</field><field name="mods.nameIdentifier">gnd:38329-6</field><field name="mods.nameIdentifier">gnd:2147083-2</field><field name="mods.nameIdentifier.top">gnd:1154322130</field><field name="mods.nameIdentifier.top">gnd:132314614</field><field name="mods.nameIdentifier.top">gnd:11370979X</field><field name="mods.nameIdentifier.top">orcid:0000-0001-9809-724X</field><field name="mods.nameIdentifier.top">gnd:38329-6</field><field name="mods.nameIdentifier.top">gnd:2147083-2</field><doc><field name="id">rosdok_disshab_0000002064-d36530e54</field><field name="mods.nameIdentifier">gnd:1154322130</field><field name="mods.name">Maksym Cherevatenko</field><field name="mods.name.top">Maksym Cherevatenko</field></doc><doc><field name="id">rosdok_disshab_0000002064-d36530e68</field><field name="mods.nameIdentifier">gnd:132314614</field><field name="mods.name">Peter Langer</field><field name="mods.name.top">Peter Langer</field></doc><doc><field name="id">rosdok_disshab_0000002064-d36530e82</field><field name="mods.nameIdentifier">gnd:11370979X</field><field name="mods.nameIdentifier">orcid:0000-0001-9809-724X</field><field name="mods.name">Thomas J. J. Müller</field><field name="mods.name.top">Thomas J. J. Müller</field></doc><doc><field name="id">rosdok_disshab_0000002064-d36530e97</field><field name="mods.nameIdentifier">gnd:38329-6</field><field name="mods.name">Universität Rostock</field><field name="mods.name.top">Universität Rostock</field></doc><doc><field name="id">rosdok_disshab_0000002064-d36530e108</field><field name="mods.nameIdentifier">gnd:2147083-2</field><field name="mods.name">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.name.top">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field></doc><field name="mods.name">Maksym Cherevatenko</field><field name="mods.name">Peter Langer</field><field name="mods.name">Thomas J. J. Müller</field><field name="mods.name">Universität Rostock</field><field name="mods.name">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.name.top">Maksym Cherevatenko</field><field name="mods.name.top">Peter Langer</field><field name="mods.name.top">Thomas J. J. Müller</field><field name="mods.name.top">Universität Rostock</field><field name="mods.name.top">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.author">Maksym Cherevatenko</field><field name="mods.place">Rostock</field><field name="mods.publisher">Universität Rostock</field><field name="mods.genre">epub.dissertation</field><field name="mods.identifier">http://purl.uni-rostock.de/rosdok/id00002414</field><field name="mods.identifier">urn:nbn:de:gbv:28-rosdok_id00002414-0</field><field name="mods.identifier">10.18453/rosdok_id00002414</field><field name="mods.subject">Chinolin</field><field name="mods.subject">Arylierung</field><field name="mods.abstract">The present thesis is mainly dedicated to the study of the synthesis of quinolines, pyrolo[2,3-b]indoles and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactions. This includes arylation of quinolines via Suzuki-Miyaura and alkynylation of 4-trifluoromethylquinolines via Sonogashira reaction. Consequent synthesis of a wide range of fused pyridines and their further modifications were successfully performed. A number of pyrolo[2,3-b]indoles and pyrimido[4,5-b]indole-2,4(3H,9H)-diones were synthesized with the usage of Buchwald-Hartwig reaction.</field><field name="mods.abstract">Die vorliegende Arbeit beschäftigt sich mit der Synthese von Chinolinen, Pyrolo[2,3-b]indolen und 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-dionen durch Palladium-katalysierte Kreuzkupplungsreaktionen. Sie beinhaltet Arylierungen von Chinolinen mittels Suzuki-Miyaura-Reaktion und Alkinylierung von 4-Trifluoromethylchinolinen mittels Sonogashira-Reaktion. Außerdem wurden verschiedene Pyrolo[2,3-b]indole und Pyrimido[4,5-b]indole-2,4(3H,9H)-dione durch Buchwald-Hartwig-Reaktion hergestellt.</field><field name="mods.dateIssued">2017</field><field name="mods.yearIssued">2017</field><field name="mods.note.statement of responsibility">vorgelegt von M. Sc. Maksym Cherevatenko</field><field name="ir.identifier">[xslt]Saxon</field><field name="recordIdentifier">rosdok/id00002414</field><field name="purl">https://purl.uni-rostock.de/rosdok/id00002414</field><field name="ppn">1049230329</field><field name="doi">10.18453/rosdok_id00002414</field><field name="urn">urn:nbn:de:gbv:28-rosdok_id00002414-0</field><field name="ir.creator.result">Maksym Cherevatenko</field><field name="ir.creator.sort">Cherevatenko Maksym</field><field name="ir.title.result">Synthesis of novel quinolines, pyrrolo[2,3-b]indoles, and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactions</field><field name="ir.doctype.result">Dissertation</field><field name="ir.doctype_en.result">doctoral thesis</field><field name="ir.originInfo.result">Universität Rostock, 2017</field><field name="ir.abstract300.result">The present thesis is mainly dedicated to the study of the synthesis of quinolines, pyrolo[2,3-b]indoles and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactions. This includes arylation of quinolines via Suzuki-Miyaura and alkynylation of…</field><field name="ir.creator_all">Maksym Cherevatenko</field><field name="ir.title_all">Synthesis of novel quinolines, pyrrolo[2,3-b]indoles, and 1H-pyrimido[4,5-b]indole-2,4(3H,9H)-diones via palladium-catalyzed cross-coupling reactions</field><field name="ir.location_all">Universitätsbibliothek Rostock</field><field name="ir.location_all">http://purl.uni-rostock.de/rosdok/id00002414</field><field name="ir.creator_all">Maksym</field><field name="ir.creator_all">Cherevatenko</field><field name="ir.creator_all">1988 -</field><field name="ir.creator_all"></field><field name="ir.creator_all">VerfasserIn</field><field name="ir.creator_all">aut</field><field name="ir.creator_all">1154322130</field><field name="ir.creator_all">Peter</field><field name="ir.creator_all">Langer</field><field name="ir.creator_all">1969 -</field><field name="ir.creator_all"></field><field name="ir.creator_all">AkademischeR BetreuerIn</field><field name="ir.creator_all">dgs</field><field name="ir.creator_all">132314614</field><field name="ir.creator_all">Thomas J. J.</field><field name="ir.creator_all">Müller</field><field name="ir.creator_all"></field><field name="ir.creator_all">AkademischeR BetreuerIn</field><field name="ir.creator_all">dgs</field><field name="ir.creator_all">11370979X</field><field name="ir.creator_all">0000-0001-9809-724X</field><field name="ir.creator_all">38329-6</field><field name="ir.creator_all">Universität Rostock</field><field name="ir.creator_all">1419 -</field><field name="ir.creator_all"></field><field name="ir.creator_all">Grad-verleihende Institution</field><field name="ir.creator_all">dgg</field><field name="ir.creator_all">2147083-2</field><field name="ir.creator_all">Universität Rostock</field><field name="ir.creator_all">Mathematisch-Naturwissenschaftliche Fakultät</field><field name="ir.creator_all"></field><field name="ir.creator_all">Grad-verleihende Institution</field><field name="ir.creator_all">dgg</field><field name="ir.identifier">[purl]http://purl.uni-rostock.de/rosdok/id00002414</field><field name="ir.identifier">[urn]urn:nbn:de:gbv:28-rosdok_id00002414-0</field><field name="ir.identifier">[doi]10.18453/rosdok_id00002414</field><field name="ir.oai.setspec.open_access">open_access</field><field name="ir.pubyear_start">2017</field><field name="ir.pubyear_end">2017</field><field name="ir.epoch_class.facet">epoch:21th_century</field><field name="ir.language_class.facet">rfc5646:en</field><field name="ir.doctype_class.facet">doctype:epub.dissertation</field><field name="ir.accesscondition_class.facet">accesscondition:openaccess</field><field name="ir.sdnb_class.facet">SDNB:540</field><field name="ir.institution_class.facet">institution:unirostock.mnf</field><field name="ir.state_class.facet">state:published</field></doc></add>