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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 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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">Development of novel pincer catalysts for the synthesis of fine chemicals using hydrogen autotransfer reactions</field><field name="mods.title.main">Development of novel pincer catalysts for the synthesis of fine chemicals using hydrogen autotransfer reactions</field><field name="mods.title.subtitle"></field><field name="mods.nameIdentifier">gnd:1213477697</field><field name="mods.nameIdentifier">gnd:112081908</field><field name="mods.nameIdentifier">orcid:0000-0001-5709-0965</field><field name="mods.nameIdentifier">gnd:115237585</field><field name="mods.nameIdentifier">gnd:38329-6</field><field name="mods.nameIdentifier">gnd:2147083-2</field><field name="mods.nameIdentifier.top">gnd:1213477697</field><field name="mods.nameIdentifier.top">gnd:112081908</field><field name="mods.nameIdentifier.top">orcid:0000-0001-5709-0965</field><field name="mods.nameIdentifier.top">gnd:115237585</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_0000002306-d3940301e54</field><field name="mods.nameIdentifier">gnd:1213477697</field><field name="mods.name">Patrick Piehl</field><field name="mods.name.top">Patrick Piehl</field></doc><doc><field name="id">rosdok_disshab_0000002306-d3940301e68</field><field name="mods.nameIdentifier">gnd:112081908</field><field name="mods.nameIdentifier">orcid:0000-0001-5709-0965</field><field name="mods.name">Matthias Beller</field><field name="mods.name.top">Matthias Beller</field></doc><doc><field name="id">rosdok_disshab_0000002306-d3940301e84</field><field name="mods.nameIdentifier">gnd:115237585</field><field name="mods.name">Wolfram Seidel</field><field name="mods.name.top">Wolfram Seidel</field></doc><doc><field name="id">rosdok_disshab_0000002306-d3940301e99</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_0000002306-d3940301e110</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">Patrick Piehl</field><field name="mods.name">Matthias Beller</field><field name="mods.name">Wolfram Seidel</field><field name="mods.name">Universität Rostock</field><field name="mods.name">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.name.top">Patrick Piehl</field><field name="mods.name.top">Matthias Beller</field><field name="mods.name.top">Wolfram Seidel</field><field name="mods.name.top">Universität Rostock</field><field name="mods.name.top">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.author">Patrick Piehl</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/id00002703</field><field name="mods.identifier">urn:nbn:de:gbv:28-rosdok_id00002703-6</field><field name="mods.identifier">10.18453/rosdok_id00002703</field><field name="mods.subject">Pincer-Ligand</field><field name="mods.subject">Katalysator</field><field name="mods.subject">Alkylierung</field><field name="mods.abstract">This thesis deals with the development of different homogeneous PNP pincer catalysts and their application in hydrogen autotransfer reactions. Manganese, rhenium and cyclometalated ruthenium complexes were used as catalysts for the α-alkylation of ketones with alcohols, a reaction creating new C‒C bonds while producing water as sole stochiometric by-product. This reaction was used for the alkylation of a broad scope of ketones including biologically relevant compounds like hormones with various alcohols.</field><field name="mods.abstract">Die vorliegende Arbeit beschäftigt sich mit der Entwicklung homogener PNP-Pincerkomplexe und deren Einsatz in Hydrogen-Autotransfer-Reaktionen. Dementsprechend wurden Mangan-, Rhenium- und cyclometallierte Rutheniumkomplexe als Katalysatoren für die α-Alkylierung von Ketonen mit Alkoholen verwendet. Bei dieser Reaktion werden neue C‒C-Bindungen geknüpft, während Wasser das einzige in stöchiometrischen Mengen anfallende Nebenprodukt darstellt. Unter Anwendung dieser Prozedur gelang die Alkylierung zahlreicher Substanzen, unter anderem auch biologisch relevanter Stoffe wie Hormone.</field><field name="mods.dateIssued">2019</field><field name="mods.yearIssued">2019</field><field name="mods.note.other">Enthält Zeitschriftenartikel</field><field name="mods.note.referee">Matthias Beller (Universität Rostock, Leibniz-Institut für Katalyse) ; Wolfram Seidel (Universität Rostock)</field><field name="mods.note.statement of responsibility">vorgelegt von Patrick Piehl</field><field name="mods.type">epub.dissertation</field><field name="search_result_link_text">1
        Piehl_Dissertation_2020.pdf
        
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        rosdok/id000027031724113364Oau2020-07-092023-08-05T19:14:51ZrdaConverted from PICA to MODS using Pica2Mods XSLT Transformer 2.7 [SCM: "0c0e7a3c226a4a0cbcbec39b493c3c5257339ab8" "v2.7" "2023-08-04T00:00:00+0200"] with mode 'DEFAULT'.DissertationHochschulschriftDevelopment of novel pincer catalysts for the synthesis of fine chemicals using hydrogen autotransfer reactionsThis thesis deals with the development of different homogeneous PNP pincer catalysts and their application in hydrogen autotransfer reactions. Manganese, rhenium and cyclometalated ruthenium complexes were used as catalysts for the α-alkylation of ketones with alcohols, a reaction creating new C‒C bonds while producing water as sole stochiometric by-product. This reaction was used for the alkylation of a broad scope of ketones including biologically relevant compounds like hormones with various alcohols.Die vorliegende Arbeit beschäftigt sich mit der Entwicklung homogener PNP-Pincerkomplexe und deren Einsatz in Hydrogen-Autotransfer-Reaktionen. Dementsprechend wurden Mangan-, Rhenium- und cyclometallierte Rutheniumkomplexe als Katalysatoren für die α-Alkylierung von Ketonen mit Alkoholen verwendet. Bei dieser Reaktion werden neue C‒C-Bindungen geknüpft, während Wasser das einzige in stöchiometrischen Mengen anfallende Nebenprodukt darstellt. Unter Anwendung dieser Prozedur gelang die Alkylierung zahlreicher Substanzen, unter anderem auch biologisch relevanter Stoffe wie Hormone.PatrickPiehl1991 -VerfasserInaut1213477697MatthiasBeller1962 -AkademischeR BetreuerIndgs1120819080000-0001-5709-0965WolframSeidel1967 -AkademischeR BetreuerIndgs11523758538329-6Universität Rostock1419 -Grad-verleihende Institutiondgg2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgghttp://purl.uni-rostock.de/rosdok/id00002703urn:nbn:de:gbv:28-rosdok_id00002703-610.18453/rosdok_id00002703540 ChemieMathematisch-Naturwissenschaftliche Fakultätalle Rechte vorbehaltenNutzungsrechte erteiltLizenz Metadaten: CC0frei zugänglich (Open Access)en2019Universität RostockRostockmonographic202020192020Universitätsbibliothek RostockRostock2020Universitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00002703Enthält ZeitschriftenartikelMatthias Beller (Universität Rostock, Leibniz-Institut für Katalyse) ; Wolfram Seidel (Universität Rostock)vorgelegt von Patrick PiehlPincer-LigandKatalysatorAlkylierung
      
    
  
  
    
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      2023-08-08T10:11:25.866Z
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      administrator</field><field name="derivateLabel">fulltext</field><field name="ir.pdffulltext_url">file/rosdok_disshab_0000002306/rosdok_derivate_0000088876/Piehl_Dissertation_2020.pdf</field><field name="mods.title">Development of novel pincer catalysts for the synthesis of fine chemicals using hydrogen autotransfer reactions</field><field name="mods.title.main">Development of novel pincer catalysts for the synthesis of fine chemicals using hydrogen autotransfer reactions</field><field name="mods.title.subtitle"></field><field name="mods.nameIdentifier">gnd:1213477697</field><field name="mods.nameIdentifier">gnd:112081908</field><field name="mods.nameIdentifier">orcid:0000-0001-5709-0965</field><field name="mods.nameIdentifier">gnd:115237585</field><field name="mods.nameIdentifier">gnd:38329-6</field><field name="mods.nameIdentifier">gnd:2147083-2</field><field name="mods.nameIdentifier.top">gnd:1213477697</field><field name="mods.nameIdentifier.top">gnd:112081908</field><field name="mods.nameIdentifier.top">orcid:0000-0001-5709-0965</field><field name="mods.nameIdentifier.top">gnd:115237585</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_0000002306-d3940301e54</field><field name="mods.nameIdentifier">gnd:1213477697</field><field name="mods.name">Patrick Piehl</field><field name="mods.name.top">Patrick Piehl</field></doc><doc><field name="id">rosdok_disshab_0000002306-d3940301e68</field><field name="mods.nameIdentifier">gnd:112081908</field><field name="mods.nameIdentifier">orcid:0000-0001-5709-0965</field><field name="mods.name">Matthias Beller</field><field name="mods.name.top">Matthias Beller</field></doc><doc><field name="id">rosdok_disshab_0000002306-d3940301e84</field><field name="mods.nameIdentifier">gnd:115237585</field><field name="mods.name">Wolfram Seidel</field><field name="mods.name.top">Wolfram Seidel</field></doc><doc><field name="id">rosdok_disshab_0000002306-d3940301e99</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_0000002306-d3940301e110</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">Patrick Piehl</field><field name="mods.name">Matthias Beller</field><field name="mods.name">Wolfram Seidel</field><field name="mods.name">Universität Rostock</field><field name="mods.name">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.name.top">Patrick Piehl</field><field name="mods.name.top">Matthias Beller</field><field name="mods.name.top">Wolfram Seidel</field><field name="mods.name.top">Universität Rostock</field><field name="mods.name.top">Universität Rostock Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.author">Patrick Piehl</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/id00002703</field><field name="mods.identifier">urn:nbn:de:gbv:28-rosdok_id00002703-6</field><field name="mods.identifier">10.18453/rosdok_id00002703</field><field name="mods.subject">Pincer-Ligand</field><field name="mods.subject">Katalysator</field><field name="mods.subject">Alkylierung</field><field name="mods.abstract">This thesis deals with the development of different homogeneous PNP pincer catalysts and their application in hydrogen autotransfer reactions. Manganese, rhenium and cyclometalated ruthenium complexes were used as catalysts for the α-alkylation of ketones with alcohols, a reaction creating new C‒C bonds while producing water as sole stochiometric by-product. This reaction was used for the alkylation of a broad scope of ketones including biologically relevant compounds like hormones with various alcohols.</field><field name="mods.abstract">Die vorliegende Arbeit beschäftigt sich mit der Entwicklung homogener PNP-Pincerkomplexe und deren Einsatz in Hydrogen-Autotransfer-Reaktionen. Dementsprechend wurden Mangan-, Rhenium- und cyclometallierte Rutheniumkomplexe als Katalysatoren für die α-Alkylierung von Ketonen mit Alkoholen verwendet. Bei dieser Reaktion werden neue C‒C-Bindungen geknüpft, während Wasser das einzige in stöchiometrischen Mengen anfallende Nebenprodukt darstellt. Unter Anwendung dieser Prozedur gelang die Alkylierung zahlreicher Substanzen, unter anderem auch biologisch relevanter Stoffe wie Hormone.</field><field name="mods.dateIssued">2019</field><field name="mods.yearIssued">2019</field><field name="mods.note.other">Enthält Zeitschriftenartikel</field><field name="mods.note.referee">Matthias Beller (Universität Rostock, Leibniz-Institut für Katalyse) ; Wolfram Seidel (Universität Rostock)</field><field name="mods.note.statement of responsibility">vorgelegt von Patrick Piehl</field><field name="ir.identifier">[xslt]Saxon</field><field name="recordIdentifier">rosdok/id00002703</field><field name="purl">https://purl.uni-rostock.de/rosdok/id00002703</field><field name="ppn">1724113364</field><field name="doi">10.18453/rosdok_id00002703</field><field name="urn">urn:nbn:de:gbv:28-rosdok_id00002703-6</field><field name="ir.creator.result">Patrick Piehl</field><field name="ir.creator.sort">Piehl Patrick</field><field name="ir.title.result">Development of novel pincer catalysts for the synthesis of fine chemicals using hydrogen autotransfer 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, 2019</field><field name="ir.abstract300.result">This thesis deals with the development of different homogeneous PNP pincer catalysts and their application in hydrogen autotransfer reactions. Manganese, rhenium and cyclometalated ruthenium complexes were used as catalysts for the α-alkylation of ketones with alcohols, a reaction creating new C‒C…</field><field name="ir.creator_all">Patrick Piehl</field><field name="ir.title_all">Development of novel pincer catalysts for the synthesis of fine chemicals using hydrogen autotransfer reactions</field><field name="ir.location_all">Universitätsbibliothek Rostock</field><field name="ir.location_all">http://purl.uni-rostock.de/rosdok/id00002703</field><field name="ir.creator_all">Patrick</field><field name="ir.creator_all">Piehl</field><field name="ir.creator_all">1991 -</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">1213477697</field><field name="ir.creator_all">Matthias</field><field name="ir.creator_all">Beller</field><field name="ir.creator_all">1962 -</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">112081908</field><field name="ir.creator_all">0000-0001-5709-0965</field><field name="ir.creator_all">Wolfram</field><field name="ir.creator_all">Seidel</field><field name="ir.creator_all">1967 -</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">115237585</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/id00002703</field><field name="ir.identifier">[urn]urn:nbn:de:gbv:28-rosdok_id00002703-6</field><field name="ir.identifier">[doi]10.18453/rosdok_id00002703</field><field name="ir.oai.setspec.open_access">open_access</field><field name="ir.pubyear_start">2019</field><field name="ir.pubyear_end">2019</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>