mycoreobjectrosdok_disshab_0000000603rosdok_disshab_0000000603rosdokdisshabrosdok_derivate_00000045572023-08-08T10:02:28.013Z2011-02-18T16:29:59.660Zadministratorpublished1rosdok_derivate_0000004557truetruederivate_types:fulltextVolltextfulltextwf_edit_epub wf_register_epubstate:publishedstate:publishedveröffentlichtpublishedrosdok/id00000807646972782MODS updated during RosDok migration in June 2021DissertationHochschulschrift143546996ImranMalik1979-VerfasserInautSynthesis of Substituted Dibenzothiophenes, Pyrazines, Quinoxalines, Flavones, Pyrimidines and Furans by Regioselective Palladium (0)-Catalyzed Cross-Coupling ReactionsenProf. Dr.PeterLangerAkademischeR BetreuerIndgsProf. Dr.LutzAckermannAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00000807http://purl.uni-rostock.de/rosdok/id00000807urn:nbn:de:gbv:28-diss2011-0030-7540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2010monographic20112010Universitätsbibliothek RostockRostock20112011The palladium(0)-catalyzed Heck reactions of brominated benzothiophene provided functionalized dibenzothiophenes by 6π-electro cyclization reactions. Heck reactions of dichloropyrazine and quinoxaline provided dialkenyl-, 2-alkenyl-3-alkyl and dialkylpyrazines and quinoxalines. Suzuki-Miyaura reactions of the bis(triflate) of 7,8- dihyroxyflavone with arylboronic acids afforded aryl-substituted flavones with excellent site-selectivity. Sonogashira reactions of tetrachloropyrimidine and tetrabromofuran provided di-, tri-, tetra-alkynylated and mixed Sonogashira-Suzuki products with excellent fluorescence properties.catalysisheterocyclicelectrocyclizationfluorescenceUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000807doctype:epubdoctype:epubDokumenttypDocument typedoctype:epub.dissertationdoctype:epub.dissertationDissertationdoctoral thesisdiniPublType:doctoralThesis diniPublType2022:PhDThesis XMetaDissPlusThesisLevel:thesis.doctoralinfo:eu-repo/semantics/doctoralThesisdocumentnatureOfContent:ppn_105825778natureOfContent:ppn_105825778HochschulschriftdiniPublType2022:DoctoralThesisdiniPublType2022:DoctoralThesisDissertation oder HabilitationDoctoral thesisDRIVERdiniPublType2022:PhDThesisdiniPublType2022:PhDThesisDissertationPhD thesisKDSF (Pu34)XMetaDissPlusThesisLevel:thesis.doctoralXMetaDissPlusThesisLevel:thesis.doctoralDoktorarbeitdoctoral thesisrfc5646:enrfc5646:enEnglischEnglishengengSDNB:540SDNB:540540 Chemie540 Chemistry & allied sciencesinstitution:unirostockinstitution:unirostockUniversität RostockUniversity of RostockUniversität RostockUniversität RostockUni.Rostockhttp://d-nb.info/gnd/38329-6institution:unirostock.mnfinstitution:unirostock.mnfMathematisch-Naturwissenschaftliche FakultätFaculty of Mathematics and Natural SciencesUniversität Rostock. Mathematisch-Naturwissenschaftliche FakultätMathematisch-Natur-<br />wissenschaftliche FakultätUni.Rostock.Fakultaet.MNFhttp://d-nb.info/gnd/2147083-2accesscondition:openaccessaccesscondition:openaccessfrei zugänglich (Open Access)open accesshttp://purl.org/coar/access_right/c_abf2OAfreeinfo:eu-repo/semantics/openAccess[DE-28]Open Access$gControlled Vocabulary for Access Rights$uhttp://purl.org/coar/access_right/c_abf2licenseinfo:metadatalicenseinfo:metadataLizenzen für Metadatenlicenseinfo:metadata.cc0licenseinfo:metadata.cc0Lizenz Metadaten: CC0license metadata: CC0/creativecommons/p/zero/1.0/88x31.pnghttps://creativecommons.org/publicdomain/zero/1.0/licenseinfo:depositlicenseinfo:depositVeröffentlichungsgenehmigungpermission to storelicenseinfo:deposit.rightsgrantedlicenseinfo:deposit.rightsgrantedNutzungsrechte erteiltrights grantedlicenseinfo:worklicenseinfo:workWerkworklicenseinfo:work.rightsreservedlicenseinfo:work.rightsreservedalle Rechte vorbehaltenall rights reserved/creativecommons/r/reserved/0.9/88x31.png[DE-28]Urheberrechtsschutz 1.0$gRights Statements$uhttp://rightsstatements.org/vocab/InC/1.0/http://rightsstatements.org/vocab/InC/1.0/http://rightsstatements.org/vocab/InC/1.0/Synthesis of Substituted Dibenzothiophenes, Pyrazines, Quinoxalines, Flavones, Pyrimidines and Furans by Regioselective Palladium (0)-Catalyzed Cross-Coupling ReactionsSynthesis of Substituted Dibenzothiophenes, Pyrazines, Quinoxalines, Flavones, Pyrimidines and Furans by Regioselective Palladium (0)-Catalyzed Cross-Coupling Reactionsgnd:143546996gnd:2147083-2gnd:143546996gnd:2147083-2rosdok_disshab_0000000603-d4885907e39gnd:143546996Imran MalikImran Malikrosdok_disshab_0000000603-d4885907e60Prof. Dr. Peter LangerProf. Dr. Peter Langerrosdok_disshab_0000000603-d4885907e72Prof. Dr. Lutz AckermannProf. Dr. Lutz Ackermannrosdok_disshab_0000000603-d4885907e84gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätImran MalikProf. Dr. Peter LangerProf. Dr. Lutz AckermannUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätImran MalikProf. Dr. Peter LangerProf. Dr. Lutz AckermannUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätImran MalikRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00000807http://purl.uni-rostock.de/rosdok/id00000807urn:nbn:de:gbv:28-diss2011-0030-7catalysisheterocyclicelectrocyclizationfluorescenceThe palladium(0)-catalyzed Heck reactions of brominated benzothiophene provided functionalized dibenzothiophenes by 6π-electro cyclization reactions. Heck reactions of dichloropyrazine and quinoxaline provided dialkenyl-, 2-alkenyl-3-alkyl and dialkylpyrazines and quinoxalines. Suzuki-Miyaura reactions of the bis(triflate) of 7,8- dihyroxyflavone with arylboronic acids afforded aryl-substituted flavones with excellent site-selectivity. Sonogashira reactions of tetrachloropyrimidine and tetrabromofuran provided di-, tri-, tetra-alkynylated and mixed Sonogashira-Suzuki products with excellent fluorescence properties.20102010epub.dissertation1 Dissertation_Malik_2011.pdf 3228759 d44f0ea6c9bbbbf505a83fe00b4c5fc3 rosdok/id00000807646972782MODS updated during RosDok migration in June 2021DissertationHochschulschrift143546996ImranMalik1979-VerfasserInautSynthesis of Substituted Dibenzothiophenes, Pyrazines, Quinoxalines, Flavones, Pyrimidines and Furans by Regioselective Palladium (0)-Catalyzed Cross-Coupling ReactionsenProf. Dr.PeterLangerAkademischeR BetreuerIndgsProf. Dr.LutzAckermannAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00000807http://purl.uni-rostock.de/rosdok/id00000807urn:nbn:de:gbv:28-diss2011-0030-7540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2010monographic20112010Universitätsbibliothek RostockRostock20112011The palladium(0)-catalyzed Heck reactions of brominated benzothiophene provided functionalized dibenzothiophenes by 6π-electro cyclization reactions. 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Heck reactions of dichloropyrazine and quinoxaline provided dialkenyl-, 2-alkenyl-3-alkyl and dialkylpyrazines and quinoxalines. Suzuki-Miyaura reactions of the bis(triflate) of 7,8- dihyroxyflavone with arylboronic acids afforded aryl-substituted flavones with excellent site-selectivity. Sonogashira reactions of tetrachloropyrimidine and tetrabromofuran provided di-, tri-, tetra-alkynylated and mixed Sonogashira-Suzuki products with excellent fluorescence properties.20102010[xslt]Saxonrosdok/id00000807https://purl.uni-rostock.de/rosdok/id0000080764697278210.18453/rosdok_id00000807urn:nbn:de:gbv:28-diss2011-0030-7Imran MalikMalik ImranSynthesis of Substituted Dibenzothiophenes, Pyrazines, Quinoxalines, Flavones, Pyrimidines and Furans by Regioselective Palladium (0)-Catalyzed Cross-Coupling ReactionsDissertationdoctoral thesisUniversität Rostock, 2010The palladium(0)-catalyzed Heck reactions of brominated benzothiophene provided functionalized dibenzothiophenes by 6π-electro cyclization reactions. Heck reactions of dichloropyrazine and quinoxaline provided dialkenyl-, 2-alkenyl-3-alkyl and dialkylpyrazines and quinoxalines. Suzuki-Miyaura…Imran MalikSynthesis of Substituted Dibenzothiophenes, Pyrazines, Quinoxalines, Flavones, Pyrimidines and Furans by Regioselective Palladium (0)-Catalyzed Cross-Coupling ReactionsUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000807143546996ImranMalik1979-VerfasserInautProf. Dr.PeterLangerAkademischeR BetreuerIndgsProf. Dr.LutzAckermannAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg[doi]10.18453/rosdok_id00000807[purl]http://purl.uni-rostock.de/rosdok/id00000807[urn]urn:nbn:de:gbv:28-diss2011-0030-7open_access20102010epoch:21th_centuryrfc5646:endoctype:epub.dissertationaccesscondition:openaccessSDNB:540institution:unirostock.mnfstate:published