<?xml version="1.0" encoding="UTF-8" standalone="yes"?><add><doc><field name="objectKind">mycoreobject</field><field name="id">rosdok_disshab_0000000102</field><field name="returnId">rosdok_disshab_0000000102</field><field name="objectProject">rosdok</field><field name="objectType">disshab</field><field name="link">rosdok_derivate_0000003634</field><field name="modified">2023-08-08T10:00:22.783Z</field><field name="created">2008-10-29T16:23:16.102Z</field><field name="modifiedby">administrator</field><field name="state">published</field><field name="derCount">1</field><field name="derivates">rosdok_derivate_0000003634</field><field name="worldReadable">true</field><field name="worldReadableComplete">true</field><field name="category">derivate_types:fulltext</field><field name="allMeta">Volltext</field><field name="allMeta">fulltext</field><field name="allMeta">wf_edit_epub wf_register_epub</field><field name="category">state:published</field><field name="category.top">state:published</field><field name="allMeta">veröffentlicht</field><field name="allMeta">published</field><field name="allMeta">rosdok/id00000362</field><field name="allMeta">585095019</field><field name="allMeta">MODS updated during RosDok migration in June 2021</field><field name="allMeta">Dissertation</field><field name="allMeta">Hochschulschrift</field><field name="allMeta">136535313</field><field name="allMeta">Karolin</field><field name="allMeta">Krüger</field><field name="allMeta">1981-</field><field name="allMeta">VerfasserIn</field><field name="allMeta">aut</field><field name="allMeta">Synthesis of Biologically Active N-Heterocycles and Amines via Catalytic Hydroamination of Alkynes</field><field name="allMeta">en</field><field name="allMeta">Prof. Dr.</field><field name="allMeta">Matthias</field><field name="allMeta">Beller</field><field name="allMeta">AkademischeR BetreuerIn</field><field name="allMeta">dgs</field><field name="allMeta">Prof. Dr.</field><field name="allMeta">Peter</field><field name="allMeta">Langer</field><field name="allMeta">AkademischeR BetreuerIn</field><field name="allMeta">dgs</field><field name="allMeta">2147083-2</field><field name="allMeta">Universität Rostock</field><field name="allMeta">Mathematisch-Naturwissenschaftliche Fakultät</field><field name="allMeta">Grad-verleihende Institution</field><field name="allMeta">dgg</field><field name="allMeta">10.18453/rosdok_id00000362</field><field name="allMeta">http://purl.uni-rostock.de/rosdok/id00000362</field><field name="allMeta">urn:nbn:de:gbv:28-diss2008-0096-0</field><field name="allMeta">540 Chemie</field><field name="allMeta">Mathematisch-Naturwissenschaftliche Fakultät</field><field name="allMeta">frei zugänglich (Open Access)</field><field name="allMeta">Lizenz Metadaten: CC0</field><field name="allMeta">Nutzungsrechte erteilt</field><field name="allMeta">alle Rechte vorbehalten</field><field name="allMeta">Universität Rostock</field><field name="allMeta">Rostock</field><field name="allMeta">2008</field><field name="allMeta">monographic</field><field name="allMeta">2008</field><field name="allMeta">2008</field><field name="allMeta">Universitätsbibliothek Rostock</field><field name="allMeta">Rostock</field><field name="allMeta">2008</field><field name="allMeta">2008</field><field name="allMeta">This thesis presents new syntheses of N-heterocycles and amines. Building up on our prior studies in titanium-catalyzed hydroamination of alkynes we discovered zinc salts as new hydroamination catalysts. Zinc chloride and zinc triflate were successfully applied in the intermolecular hydroamination of terminal alkynes for the synthesis of various substituted indole derivatives, pyrazolines and pyrazoles, pyridazinones as well as amines. Additional functionalization reactions on special synthesized indole structures lead to pharmaceutically and biologically interesting substances.</field><field name="allMeta">indole</field><field name="allMeta">hydroamination</field><field name="allMeta">zinc</field><field name="allMeta">Universitätsbibliothek Rostock</field><field name="allMeta">http://purl.uni-rostock.de/rosdok/id00000362</field><field name="category">doctype:epub</field><field name="category.top">doctype:epub</field><field name="allMeta">Dokumenttyp</field><field name="allMeta">Document type</field><field name="category">doctype:epub.dissertation</field><field name="category.top">doctype:epub.dissertation</field><field name="allMeta">Dissertation</field><field name="allMeta">doctoral thesis</field><field name="allMeta">diniPublType:doctoralThesis diniPublType2022:PhDThesis XMetaDissPlusThesisLevel:thesis.doctoral</field><field name="allMeta">info:eu-repo/semantics/doctoralThesis</field><field name="allMeta">document</field><field name="category">natureOfContent:ppn_105825778</field><field name="category.top">natureOfContent:ppn_105825778</field><field name="allMeta">Hochschulschrift</field><field name="category">diniPublType2022:DoctoralThesis</field><field name="category.top">diniPublType2022:DoctoralThesis</field><field name="allMeta">Dissertation oder Habilitation</field><field name="allMeta">Doctoral thesis</field><field name="allMeta">DRIVER</field><field name="category">diniPublType2022:PhDThesis</field><field name="category.top">diniPublType2022:PhDThesis</field><field name="allMeta">Dissertation</field><field name="allMeta">PhD thesis</field><field name="allMeta">KDSF (Pu34)</field><field name="category">XMetaDissPlusThesisLevel:thesis.doctoral</field><field name="category.top">XMetaDissPlusThesisLevel:thesis.doctoral</field><field name="allMeta">Doktorarbeit</field><field name="allMeta">doctoral thesis</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="category">SDNB:540</field><field name="category.top">SDNB:540</field><field name="allMeta">540 Chemie</field><field name="allMeta">540 Chemistry &amp; allied sciences</field><field name="category">institution:unirostock</field><field name="category.top">institution:unirostock</field><field name="allMeta">Universität Rostock</field><field name="allMeta">University of Rostock</field><field name="allMeta">Universität Rostock</field><field name="allMeta">Universität Rostock</field><field name="allMeta">Uni.Rostock</field><field name="allMeta">http://d-nb.info/gnd/38329-6</field><field name="category">institution:unirostock.mnf</field><field name="category.top">institution:unirostock.mnf</field><field name="allMeta">Mathematisch-Naturwissenschaftliche Fakultät</field><field name="allMeta">Faculty of Mathematics and Natural Sciences</field><field name="allMeta">Universität Rostock. 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">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">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">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: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="mods.title">Synthesis of Biologically Active N-Heterocycles and Amines via Catalytic Hydroamination of Alkynes</field><field name="mods.title.main">Synthesis of Biologically Active N-Heterocycles and Amines via Catalytic Hydroamination of Alkynes</field><field name="mods.title.subtitle"></field><field name="mods.nameIdentifier">gnd:136535313</field><field name="mods.nameIdentifier">gnd:2147083-2</field><field name="mods.nameIdentifier.top">gnd:136535313</field><field name="mods.nameIdentifier.top">gnd:2147083-2</field><doc><field name="id">rosdok_disshab_0000000102-d2476406e39</field><field name="mods.nameIdentifier">gnd:136535313</field><field name="mods.name">Karolin Krüger</field><field name="mods.name.top">Karolin Krüger</field></doc><doc><field name="id">rosdok_disshab_0000000102-d2476406e60</field><field name="mods.name">Prof. Dr. Matthias Beller</field><field name="mods.name.top">Prof. Dr. Matthias Beller</field></doc><doc><field name="id">rosdok_disshab_0000000102-d2476406e72</field><field name="mods.name">Prof. Dr. Peter Langer</field><field name="mods.name.top">Prof. Dr. Peter Langer</field></doc><doc><field name="id">rosdok_disshab_0000000102-d2476406e84</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">Karolin Krüger</field><field name="mods.name">Prof. Dr. Matthias Beller</field><field name="mods.name">Prof. Dr. Peter Langer</field><field name="mods.name">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.name.top">Karolin Krüger</field><field name="mods.name.top">Prof. Dr. Matthias Beller</field><field name="mods.name.top">Prof. Dr. Peter Langer</field><field name="mods.name.top">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.author">Karolin Krüger</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">10.18453/rosdok_id00000362</field><field name="mods.identifier">http://purl.uni-rostock.de/rosdok/id00000362</field><field name="mods.identifier">urn:nbn:de:gbv:28-diss2008-0096-0</field><field name="mods.subject">indole</field><field name="mods.subject">hydroamination</field><field name="mods.subject">zinc</field><field name="mods.abstract">This thesis presents new syntheses of N-heterocycles and amines. Building up on our prior studies in titanium-catalyzed hydroamination of alkynes we discovered zinc salts as new hydroamination catalysts. Zinc chloride and zinc triflate were successfully applied in the intermolecular hydroamination of terminal alkynes for the synthesis of various substituted indole derivatives, pyrazolines and pyrazoles, pyridazinones as well as amines. Additional functionalization reactions on special synthesized indole structures lead to pharmaceutically and biologically interesting substances.</field><field name="mods.dateIssued">2008</field><field name="mods.yearIssued">2008</field><field name="mods.type">epub.dissertation</field><field name="search_result_link_text">1
        Dissertation_Krueger_2008.pdf
        
        1760657
        072069ccd16d7e9d26fcbcbe108961a0
      
    
  
  
    
      
        rosdok/id00000362585095019MODS updated during RosDok migration in June 2021DissertationHochschulschrift136535313KarolinKrüger1981-VerfasserInautSynthesis of Biologically Active N-Heterocycles and Amines via Catalytic Hydroamination of AlkynesenProf. Dr.MatthiasBellerAkademischeR BetreuerIndgsProf. Dr.PeterLangerAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00000362http://purl.uni-rostock.de/rosdok/id00000362urn:nbn:de:gbv:28-diss2008-0096-0540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2008monographic20082008Universitätsbibliothek RostockRostock20082008This thesis presents new syntheses of N-heterocycles and amines. Building up on our prior studies in titanium-catalyzed hydroamination of alkynes we discovered zinc salts as new hydroamination catalysts. Zinc chloride and zinc triflate were successfully applied in the intermolecular hydroamination of terminal alkynes for the synthesis of various substituted indole derivatives, pyrazolines and pyrazoles, pyridazinones as well as amines. Additional functionalization reactions on special synthesized indole structures lead to pharmaceutically and biologically interesting substances.indolehydroaminationzincUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000362
      
    
  
  
    
      2008-10-29T16:23:16.102Z
      2023-08-08T10:00:22.783Z
      2023-08-18T10:00:22.787Z
    
    
      {"identifier":"rosdok/id00000362","type":"local_id","additional":"","service":"MCRLocalID","created":"2018-06-30T12:33:56.083Z"}
      {"identifier":"http://purl.uni-rostock.de/rosdok/id00000362","type":"purl","additional":"","service":"RosDokPURL","created":"2018-06-30T12:33:56.272Z","registered":"2018-06-30T12:33:56.272Z"}
      {"identifier":"10.18453/rosdok_id00000362","type":"doi","additional":"","service":"RosDokDOI","created":"2018-06-30T12:33:57.624Z","registered":"2018-06-30T12:33:57.624Z"}
      {"identifier":"urn:nbn:de:gbv:28-diss2008-0096-0","type":"dnbUrn","additional":"","service":"RosDokURN","created":"2018-06-30T12:33:56.087Z","registered":"2008-11-20T03:17:17.870Z"}
      administrator</field><field name="derivateLabel">fulltext</field><field name="ir.pdffulltext_url">file/rosdok_disshab_0000000102/rosdok_derivate_0000003634/Dissertation_Krueger_2008.pdf</field><field name="mods.title">Synthesis of Biologically Active N-Heterocycles and Amines via Catalytic Hydroamination of Alkynes</field><field name="mods.title.main">Synthesis of Biologically Active N-Heterocycles and Amines via Catalytic Hydroamination of Alkynes</field><field name="mods.title.subtitle"></field><field name="mods.nameIdentifier">gnd:136535313</field><field name="mods.nameIdentifier">gnd:2147083-2</field><field name="mods.nameIdentifier.top">gnd:136535313</field><field name="mods.nameIdentifier.top">gnd:2147083-2</field><doc><field name="id">rosdok_disshab_0000000102-d2476406e39</field><field name="mods.nameIdentifier">gnd:136535313</field><field name="mods.name">Karolin Krüger</field><field name="mods.name.top">Karolin Krüger</field></doc><doc><field name="id">rosdok_disshab_0000000102-d2476406e60</field><field name="mods.name">Prof. Dr. Matthias Beller</field><field name="mods.name.top">Prof. Dr. Matthias Beller</field></doc><doc><field name="id">rosdok_disshab_0000000102-d2476406e72</field><field name="mods.name">Prof. Dr. Peter Langer</field><field name="mods.name.top">Prof. Dr. Peter Langer</field></doc><doc><field name="id">rosdok_disshab_0000000102-d2476406e84</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">Karolin Krüger</field><field name="mods.name">Prof. Dr. Matthias Beller</field><field name="mods.name">Prof. Dr. Peter Langer</field><field name="mods.name">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.name.top">Karolin Krüger</field><field name="mods.name.top">Prof. Dr. Matthias Beller</field><field name="mods.name.top">Prof. Dr. Peter Langer</field><field name="mods.name.top">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.author">Karolin Krüger</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">10.18453/rosdok_id00000362</field><field name="mods.identifier">http://purl.uni-rostock.de/rosdok/id00000362</field><field name="mods.identifier">urn:nbn:de:gbv:28-diss2008-0096-0</field><field name="mods.subject">indole</field><field name="mods.subject">hydroamination</field><field name="mods.subject">zinc</field><field name="mods.abstract">This thesis presents new syntheses of N-heterocycles and amines. Building up on our prior studies in titanium-catalyzed hydroamination of alkynes we discovered zinc salts as new hydroamination catalysts. Zinc chloride and zinc triflate were successfully applied in the intermolecular hydroamination of terminal alkynes for the synthesis of various substituted indole derivatives, pyrazolines and pyrazoles, pyridazinones as well as amines. Additional functionalization reactions on special synthesized indole structures lead to pharmaceutically and biologically interesting substances.</field><field name="mods.dateIssued">2008</field><field name="mods.yearIssued">2008</field><field name="ir.identifier">[xslt]Saxon</field><field name="recordIdentifier">rosdok/id00000362</field><field name="purl">https://purl.uni-rostock.de/rosdok/id00000362</field><field name="ppn">585095019</field><field name="doi">10.18453/rosdok_id00000362</field><field name="urn">urn:nbn:de:gbv:28-diss2008-0096-0</field><field name="ir.creator.result">Karolin Krüger</field><field name="ir.creator.sort">Krüger Karolin</field><field name="ir.title.result">Synthesis of Biologically Active N-Heterocycles and Amines via Catalytic Hydroamination of Alkynes</field><field name="ir.doctype.result">Dissertation</field><field name="ir.doctype_en.result">doctoral thesis</field><field name="ir.originInfo.result">Universität Rostock, 2008</field><field name="ir.abstract300.result">This thesis presents new syntheses of N-heterocycles and amines. Building up on our prior studies in titanium-catalyzed hydroamination of alkynes we discovered zinc salts as new hydroamination catalysts. Zinc chloride and zinc triflate were successfully applied in the intermolecular hydroamination…</field><field name="ir.creator_all">Karolin Krüger</field><field name="ir.title_all">Synthesis of Biologically Active N-Heterocycles and Amines via Catalytic Hydroamination of Alkynes</field><field name="ir.location_all">Universitätsbibliothek Rostock</field><field name="ir.location_all">http://purl.uni-rostock.de/rosdok/id00000362</field><field name="ir.creator_all">136535313</field><field name="ir.creator_all">Karolin</field><field name="ir.creator_all">Krüger</field><field name="ir.creator_all">1981-</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">Prof. Dr.</field><field name="ir.creator_all">Matthias</field><field name="ir.creator_all">Beller</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">Prof. Dr.</field><field name="ir.creator_all">Peter</field><field name="ir.creator_all">Langer</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">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">[doi]10.18453/rosdok_id00000362</field><field name="ir.identifier">[purl]http://purl.uni-rostock.de/rosdok/id00000362</field><field name="ir.identifier">[urn]urn:nbn:de:gbv:28-diss2008-0096-0</field><field name="ir.oai.setspec.open_access">open_access</field><field name="ir.pubyear_start">2008</field><field name="ir.pubyear_end">2008</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>