mycoreobjectrosdok_disshab_0000001869rosdok_disshab_0000001869rosdokdisshabrosdok_derivate_00000384712023-08-08T10:08:44.911Z2018-03-23T09:49:04.595ZadministratoreditorDpublished1rosdok_derivate_0000038471truetruederivate_types:fulltextVolltextfulltextwf_edit_epub wf_register_epubstate:publishedstate:publishedveröffentlichtpublishedrosdok/id000020471018341501MODS updated during RosDok migration in June 2021DissertationHochschulschrift1127072730Ngo NghiaPham1984-VerfasserInautPalladium-catalyzed synthesis of pyrrole-, indole- and phenanthridine-fused polycyclic aromatic compounds from ortho-dihaloarenesen132314614Prof. Dr. Dr. h. c. mult.PeterLangerUniversität Rostock, Institut für ChemieAkademischeR BetreuerIndgs13280252Xapl. Prof. Dr. rer. nat. habil.AndreasSchmidtUniversität Clausthal, Institut für Organische ChemieAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00002047http://purl.uni-rostock.de/rosdok/id00002047urn:nbn:de:gbv:28-diss2018-0041-4540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2018monographic20172018Universitätsbibliothek RostockRostock20182018Convenient palladium-catalyzed syntheses of polycyclic nitrogen heterocycles from ortho-dihaloarenes were developed. First, syntheses of pyrrole-fused derivatives via domino C-C/C-N coupling of ortho-dihaloarenes with imines were accomplished. Employment of ortho-dihaloarenes for sequential regioselective Suzuki reaction/double C-N coupling afforded corresponding indole-fused structures. Finally, syntheses of previously unexplored phenanthridine-fused architectures by regioselective Sonogashira reaction followed by domino or one-pot C-N coupling/hydroamination/C-H arylation were described.palladium-catalyzedcross-couplingdomino reactionUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00002047doctype: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/Palladium-catalyzed synthesis of pyrrole-, indole- and phenanthridine-fused polycyclic aromatic compounds from ortho-dihaloarenesPalladium-catalyzed synthesis of pyrrole-, indole- and phenanthridine-fused polycyclic aromatic compounds from ortho-dihaloarenesgnd:1127072730gnd:132314614gnd:13280252Xgnd:2147083-2gnd:1127072730gnd:132314614gnd:13280252Xgnd:2147083-2rosdok_disshab_0000001869-d554883e39gnd:1127072730Ngo Nghia PhamNgo Nghia Phamrosdok_disshab_0000001869-d554883e60gnd:132314614Prof. Dr. Dr. h. c. mult. Peter LangerProf. Dr. Dr. h. c. mult. Peter Langerrosdok_disshab_0000001869-d554883e75gnd:13280252Xapl. Prof. Dr. rer. nat. habil. Andreas Schmidtapl. Prof. Dr. rer. nat. habil. Andreas Schmidtrosdok_disshab_0000001869-d554883e90gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätNgo Nghia PhamProf. Dr. Dr. h. c. mult. Peter Langerapl. Prof. Dr. rer. nat. habil. Andreas SchmidtUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätNgo Nghia PhamProf. Dr. Dr. h. c. mult. Peter Langerapl. Prof. Dr. rer. nat. habil. Andreas SchmidtUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätNgo Nghia PhamRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00002047http://purl.uni-rostock.de/rosdok/id00002047urn:nbn:de:gbv:28-diss2018-0041-4palladium-catalyzedcross-couplingdomino reactionConvenient palladium-catalyzed syntheses of polycyclic nitrogen heterocycles from ortho-dihaloarenes were developed. First, syntheses of pyrrole-fused derivatives via domino C-C/C-N coupling of ortho-dihaloarenes with imines were accomplished. Employment of ortho-dihaloarenes for sequential regioselective Suzuki reaction/double C-N coupling afforded corresponding indole-fused structures. Finally, syntheses of previously unexplored phenanthridine-fused architectures by regioselective Sonogashira reaction followed by domino or one-pot C-N coupling/hydroamination/C-H arylation were described.20182018epub.dissertation1 Dissertation_Pham_2018.pdf 6319553 952458fd326d3c0e462c8caf4e83dfd4 rosdok/id000020471018341501MODS updated during RosDok migration in June 2021DissertationHochschulschrift1127072730Ngo NghiaPham1984-VerfasserInautPalladium-catalyzed synthesis of pyrrole-, indole- and phenanthridine-fused polycyclic aromatic compounds from ortho-dihaloarenesen132314614Prof. Dr. Dr. h. c. mult.PeterLangerUniversität Rostock, Institut für ChemieAkademischeR BetreuerIndgs13280252Xapl. Prof. Dr. rer. nat. habil.AndreasSchmidtUniversität Clausthal, Institut für Organische ChemieAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00002047http://purl.uni-rostock.de/rosdok/id00002047urn:nbn:de:gbv:28-diss2018-0041-4540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2018monographic20172018Universitätsbibliothek RostockRostock20182018Convenient palladium-catalyzed syntheses of polycyclic nitrogen heterocycles from ortho-dihaloarenes were developed. First, syntheses of pyrrole-fused derivatives via domino C-C/C-N coupling of ortho-dihaloarenes with imines were accomplished. Employment of ortho-dihaloarenes for sequential regioselective Suzuki reaction/double C-N coupling afforded corresponding indole-fused structures. Finally, syntheses of previously unexplored phenanthridine-fused architectures by regioselective Sonogashira reaction followed by domino or one-pot C-N coupling/hydroamination/C-H arylation were described.palladium-catalyzedcross-couplingdomino reactionUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00002047 2018-03-23T09:49:04.595Z 2023-08-08T10:08:44.911Z 2023-08-18T10:08:44.915Z editorD {"identifier":"rosdok/id00002047","type":"local_id","additional":"","service":"MCRLocalID","created":"2018-06-30T13:34:32.614Z"} {"identifier":"http://purl.uni-rostock.de/rosdok/id00002047","type":"purl","additional":"","service":"RosDokPURL","created":"2018-06-30T13:34:32.789Z","registered":"2018-06-30T13:34:32.789Z"} {"identifier":"10.18453/rosdok_id00002047","type":"doi","additional":"","service":"RosDokDOI","created":"2018-06-30T13:34:34.124Z","registered":"2018-06-30T13:34:34.124Z"} {"identifier":"urn:nbn:de:gbv:28-diss2018-0041-4","type":"dnbUrn","additional":"","service":"RosDokURN","created":"2018-06-30T13:34:32.621Z","registered":"2018-04-12T02:25:38.557Z"} administratorfulltextfile/rosdok_disshab_0000001869/rosdok_derivate_0000038471/Dissertation_Pham_2018.pdfPalladium-catalyzed synthesis of pyrrole-, indole- and phenanthridine-fused polycyclic aromatic compounds from ortho-dihaloarenesPalladium-catalyzed synthesis of pyrrole-, indole- and phenanthridine-fused polycyclic aromatic compounds from ortho-dihaloarenesgnd:1127072730gnd:132314614gnd:13280252Xgnd:2147083-2gnd:1127072730gnd:132314614gnd:13280252Xgnd:2147083-2rosdok_disshab_0000001869-d554883e39gnd:1127072730Ngo Nghia PhamNgo Nghia Phamrosdok_disshab_0000001869-d554883e60gnd:132314614Prof. Dr. Dr. h. c. mult. Peter LangerProf. Dr. Dr. h. c. mult. Peter Langerrosdok_disshab_0000001869-d554883e75gnd:13280252Xapl. Prof. Dr. rer. nat. habil. Andreas Schmidtapl. Prof. Dr. rer. nat. habil. Andreas Schmidtrosdok_disshab_0000001869-d554883e90gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätNgo Nghia PhamProf. Dr. Dr. h. c. mult. Peter Langerapl. Prof. Dr. rer. nat. habil. Andreas SchmidtUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätNgo Nghia PhamProf. Dr. Dr. h. c. mult. Peter Langerapl. Prof. Dr. rer. nat. habil. Andreas SchmidtUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätNgo Nghia PhamRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00002047http://purl.uni-rostock.de/rosdok/id00002047urn:nbn:de:gbv:28-diss2018-0041-4palladium-catalyzedcross-couplingdomino reactionConvenient palladium-catalyzed syntheses of polycyclic nitrogen heterocycles from ortho-dihaloarenes were developed. First, syntheses of pyrrole-fused derivatives via domino C-C/C-N coupling of ortho-dihaloarenes with imines were accomplished. Employment of ortho-dihaloarenes for sequential regioselective Suzuki reaction/double C-N coupling afforded corresponding indole-fused structures. Finally, syntheses of previously unexplored phenanthridine-fused architectures by regioselective Sonogashira reaction followed by domino or one-pot C-N coupling/hydroamination/C-H arylation were described.20182018[xslt]Saxonrosdok/id00002047https://purl.uni-rostock.de/rosdok/id00002047101834150110.18453/rosdok_id00002047urn:nbn:de:gbv:28-diss2018-0041-4Ngo Nghia PhamPham Ngo NghiaPalladium-catalyzed synthesis of pyrrole-, indole- and phenanthridine-fused polycyclic aromatic compounds from ortho-dihaloarenesDissertationdoctoral thesisUniversität Rostock, 2018Convenient palladium-catalyzed syntheses of polycyclic nitrogen heterocycles from ortho-dihaloarenes were developed. First, syntheses of pyrrole-fused derivatives via domino C-C/C-N coupling of ortho-dihaloarenes with imines were accomplished. Employment of ortho-dihaloarenes for sequential…Ngo Nghia PhamPalladium-catalyzed synthesis of pyrrole-, indole- and phenanthridine-fused polycyclic aromatic compounds from ortho-dihaloarenesUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id000020471127072730Ngo NghiaPham1984-VerfasserInaut132314614Prof. Dr. Dr. h. c. mult.PeterLangerUniversität Rostock, Institut für ChemieAkademischeR BetreuerIndgs13280252Xapl. Prof. Dr. rer. nat. habil.AndreasSchmidtUniversität Clausthal, Institut für Organische ChemieAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg[doi]10.18453/rosdok_id00002047[purl]http://purl.uni-rostock.de/rosdok/id00002047[urn]urn:nbn:de:gbv:28-diss2018-0041-4open_access20182018epoch:21th_centuryrfc5646:endoctype:epub.dissertationaccesscondition:openaccessSDNB:540institution:unirostock.mnfstate:published