mycoreobjectrosdok_disshab_0000000800rosdok_disshab_0000000800rosdokdisshabrosdok_derivate_00000048192023-08-08T10:03:15.288Z2012-03-03T10:22:25.602Zadministratorpublished1rosdok_derivate_0000004819truetruederivate_types:fulltextVolltextfulltextwf_edit_epub wf_register_epubstate:publishedstate:publishedveröffentlichtpublishedrosdok/id00000983687890411MODS updated during RosDok migration in June 2021DissertationHochschulschrift1020214058Ghazwan AliSalman1979-VerfasserInautSynthesis of Functionalized Benzofurans, Diaryl-Substituted 1,2,3,4-Tetrahydro-9,10-Anthracen-1-ones, 5,10-Diaryl-11Hbenzo[b]fluoren-11-ones, Benzothieno[3,2-b]quinolines, Thieno[3,2-b]pyrroles, Benzofuro[3,2-b]quinolines, and Furo[3,2-b]quinolines by Regioselective Palladium(0)-Catalyzed Cross-Coupling and Domino C-N Coupling/Annulation ReactionsenProf. Dr. Dr. h. c.PeterLangerAkademischeR BetreuerIndgsProf. Dr.SabineMüllerAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00000983http://purl.uni-rostock.de/rosdok/id00000983urn:nbn:de:gbv:28-diss2012-0018-7540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2011monographic20122011Universitätsbibliothek RostockRostock20122012The palladium(0)-catalyzed Heck cross-coupling and suzuki-Miyaura reactions of 2,3-dibromo-5-(ethoxycarbonyl)-furan, bis(triflate) of 1,2,3,4-tetrahydro-9,10-dihydroxyanthracen-1-one, and 5,10-dihydroxy-11H-benzo[b]fluoren-11-one, afforded different diarylation compounds. The palladium catalyzed reaction of 2-alkynyl-3-bromothiophenes, 2-alkynyl-3-bromobenzothiophene, 2-alkynyl-3-bromofurans, and 2-alkynyl-3-bromobenzofurans with anilines afforded thienopyrroles, benzothienoquinolines, fuoroquinoline, and benzofuoroquinolines, respectively by a domino C-N coupling / annulations and hydroamination reactions.palladiumHeckcatalystUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000983doctype: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 Functionalized Benzofurans, Diaryl-Substituted 1,2,3,4-Tetrahydro-9,10-Anthracen-1-ones, 5,10-Diaryl-11Hbenzo[b]fluoren-11-ones, Benzothieno[3,2-b]quinolines, Thieno[3,2-b]pyrroles, Benzofuro[3,2-b]quinolines, and Furo[3,2-b]quinolines by Regioselective Palladium(0)-Catalyzed Cross-Coupling and Domino C-N Coupling/Annulation ReactionsSynthesis of Functionalized Benzofurans, Diaryl-Substituted 1,2,3,4-Tetrahydro-9,10-Anthracen-1-ones, 5,10-Diaryl-11Hbenzo[b]fluoren-11-ones, Benzothieno[3,2-b]quinolines, Thieno[3,2-b]pyrroles, Benzofuro[3,2-b]quinolines, and Furo[3,2-b]quinolines by Regioselective Palladium(0)-Catalyzed Cross-Coupling and Domino C-N Coupling/Annulation Reactionsgnd:1020214058gnd:2147083-2gnd:1020214058gnd:2147083-2rosdok_disshab_0000000800-d554240e39gnd:1020214058Ghazwan Ali SalmanGhazwan Ali Salmanrosdok_disshab_0000000800-d554240e60Prof. Dr. Dr. h. c. Peter LangerProf. Dr. Dr. h. c. Peter Langerrosdok_disshab_0000000800-d554240e72Prof. Dr. Sabine MüllerProf. Dr. Sabine Müllerrosdok_disshab_0000000800-d554240e84gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätGhazwan Ali SalmanProf. Dr. Dr. h. c. Peter LangerProf. Dr. Sabine MüllerUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätGhazwan Ali SalmanProf. Dr. Dr. h. c. Peter LangerProf. Dr. Sabine MüllerUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätGhazwan Ali SalmanRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00000983http://purl.uni-rostock.de/rosdok/id00000983urn:nbn:de:gbv:28-diss2012-0018-7palladiumHeckcatalystThe palladium(0)-catalyzed Heck cross-coupling and suzuki-Miyaura reactions of 2,3-dibromo-5-(ethoxycarbonyl)-furan, bis(triflate) of 1,2,3,4-tetrahydro-9,10-dihydroxyanthracen-1-one, and 5,10-dihydroxy-11H-benzo[b]fluoren-11-one, afforded different diarylation compounds. The palladium catalyzed reaction of 2-alkynyl-3-bromothiophenes, 2-alkynyl-3-bromobenzothiophene, 2-alkynyl-3-bromofurans, and 2-alkynyl-3-bromobenzofurans with anilines afforded thienopyrroles, benzothienoquinolines, fuoroquinoline, and benzofuoroquinolines, respectively by a domino C-N coupling / annulations and hydroamination reactions.20112011epub.dissertation1 Dissertation_Salman_2012.pdf 2662266 f8f72260a699e49026d50f2db4e37ba7 rosdok/id00000983687890411MODS updated during RosDok migration in June 2021DissertationHochschulschrift1020214058Ghazwan AliSalman1979-VerfasserInautSynthesis of Functionalized Benzofurans, Diaryl-Substituted 1,2,3,4-Tetrahydro-9,10-Anthracen-1-ones, 5,10-Diaryl-11Hbenzo[b]fluoren-11-ones, Benzothieno[3,2-b]quinolines, Thieno[3,2-b]pyrroles, Benzofuro[3,2-b]quinolines, and Furo[3,2-b]quinolines by Regioselective Palladium(0)-Catalyzed Cross-Coupling and Domino C-N Coupling/Annulation ReactionsenProf. Dr. Dr. h. c.PeterLangerAkademischeR BetreuerIndgsProf. Dr.SabineMüllerAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00000983http://purl.uni-rostock.de/rosdok/id00000983urn:nbn:de:gbv:28-diss2012-0018-7540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2011monographic20122011Universitätsbibliothek RostockRostock20122012The palladium(0)-catalyzed Heck cross-coupling and suzuki-Miyaura reactions of 2,3-dibromo-5-(ethoxycarbonyl)-furan, bis(triflate) of 1,2,3,4-tetrahydro-9,10-dihydroxyanthracen-1-one, and 5,10-dihydroxy-11H-benzo[b]fluoren-11-one, afforded different diarylation compounds. The palladium catalyzed reaction of 2-alkynyl-3-bromothiophenes, 2-alkynyl-3-bromobenzothiophene, 2-alkynyl-3-bromofurans, and 2-alkynyl-3-bromobenzofurans with anilines afforded thienopyrroles, benzothienoquinolines, fuoroquinoline, and benzofuoroquinolines, respectively by a domino C-N coupling / annulations and hydroamination reactions.palladiumHeckcatalystUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000983 2012-03-03T10:22:25.602Z 2023-08-08T10:03:15.288Z 2023-08-18T10:03:15.292Z {"identifier":"rosdok/id00000983","type":"local_id","additional":"","service":"MCRLocalID","created":"2018-06-30T12:56:28.199Z"} {"identifier":"http://purl.uni-rostock.de/rosdok/id00000983","type":"purl","additional":"","service":"RosDokPURL","created":"2018-06-30T12:56:28.398Z","registered":"2018-06-30T12:56:28.398Z"} {"identifier":"10.18453/rosdok_id00000983","type":"doi","additional":"","service":"RosDokDOI","created":"2018-06-30T12:56:29.776Z","registered":"2018-06-30T12:56:29.776Z"} {"identifier":"urn:nbn:de:gbv:28-diss2012-0018-7","type":"dnbUrn","additional":"","service":"RosDokURN","created":"2018-06-30T12:56:28.204Z","registered":"2012-03-04T03:28:07.540Z"} administratorfulltextfile/rosdok_disshab_0000000800/rosdok_derivate_0000004819/Dissertation_Salman_2012.pdfSynthesis of Functionalized Benzofurans, Diaryl-Substituted 1,2,3,4-Tetrahydro-9,10-Anthracen-1-ones, 5,10-Diaryl-11Hbenzo[b]fluoren-11-ones, Benzothieno[3,2-b]quinolines, Thieno[3,2-b]pyrroles, Benzofuro[3,2-b]quinolines, and Furo[3,2-b]quinolines by Regioselective Palladium(0)-Catalyzed Cross-Coupling and Domino C-N Coupling/Annulation ReactionsSynthesis of Functionalized Benzofurans, Diaryl-Substituted 1,2,3,4-Tetrahydro-9,10-Anthracen-1-ones, 5,10-Diaryl-11Hbenzo[b]fluoren-11-ones, Benzothieno[3,2-b]quinolines, Thieno[3,2-b]pyrroles, Benzofuro[3,2-b]quinolines, and Furo[3,2-b]quinolines by Regioselective Palladium(0)-Catalyzed Cross-Coupling and Domino C-N Coupling/Annulation Reactionsgnd:1020214058gnd:2147083-2gnd:1020214058gnd:2147083-2rosdok_disshab_0000000800-d554240e39gnd:1020214058Ghazwan Ali SalmanGhazwan Ali Salmanrosdok_disshab_0000000800-d554240e60Prof. Dr. Dr. h. c. Peter LangerProf. Dr. Dr. h. c. Peter Langerrosdok_disshab_0000000800-d554240e72Prof. Dr. Sabine MüllerProf. Dr. Sabine Müllerrosdok_disshab_0000000800-d554240e84gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätGhazwan Ali SalmanProf. Dr. Dr. h. c. Peter LangerProf. Dr. Sabine MüllerUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätGhazwan Ali SalmanProf. Dr. Dr. h. c. Peter LangerProf. Dr. Sabine MüllerUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätGhazwan Ali SalmanRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00000983http://purl.uni-rostock.de/rosdok/id00000983urn:nbn:de:gbv:28-diss2012-0018-7palladiumHeckcatalystThe palladium(0)-catalyzed Heck cross-coupling and suzuki-Miyaura reactions of 2,3-dibromo-5-(ethoxycarbonyl)-furan, bis(triflate) of 1,2,3,4-tetrahydro-9,10-dihydroxyanthracen-1-one, and 5,10-dihydroxy-11H-benzo[b]fluoren-11-one, afforded different diarylation compounds. The palladium catalyzed reaction of 2-alkynyl-3-bromothiophenes, 2-alkynyl-3-bromobenzothiophene, 2-alkynyl-3-bromofurans, and 2-alkynyl-3-bromobenzofurans with anilines afforded thienopyrroles, benzothienoquinolines, fuoroquinoline, and benzofuoroquinolines, respectively by a domino C-N coupling / annulations and hydroamination reactions.20112011[xslt]Saxonrosdok/id00000983https://purl.uni-rostock.de/rosdok/id0000098368789041110.18453/rosdok_id00000983urn:nbn:de:gbv:28-diss2012-0018-7Ghazwan Ali SalmanSalman Ghazwan AliSynthesis of Functionalized Benzofurans, Diaryl-Substituted 1,2,3,4-Tetrahydro-9,10-Anthracen-1-ones, 5,10-Diaryl-11Hbenzo[b]fluoren-11-ones, Benzothieno[3,2-b]quinolines, Thieno[3,2-b]pyrroles, Benzofuro[3,2-b]quinolines, and Furo[3,2-b]quinolines by Regioselective Palladium(0)-Catalyzed Cross-Coupling and Domino C-N Coupling/Annulation ReactionsDissertationdoctoral thesisUniversität Rostock, 2011The palladium(0)-catalyzed Heck cross-coupling and suzuki-Miyaura reactions of 2,3-dibromo-5-(ethoxycarbonyl)-furan, bis(triflate) of 1,2,3,4-tetrahydro-9,10-dihydroxyanthracen-1-one, and 5,10-dihydroxy-11H-benzo[b]fluoren-11-one, afforded different diarylation compounds. The palladium catalyzed…Ghazwan Ali SalmanSynthesis of Functionalized Benzofurans, Diaryl-Substituted 1,2,3,4-Tetrahydro-9,10-Anthracen-1-ones, 5,10-Diaryl-11Hbenzo[b]fluoren-11-ones, Benzothieno[3,2-b]quinolines, Thieno[3,2-b]pyrroles, Benzofuro[3,2-b]quinolines, and Furo[3,2-b]quinolines by Regioselective Palladium(0)-Catalyzed Cross-Coupling and Domino C-N Coupling/Annulation ReactionsUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id000009831020214058Ghazwan AliSalman1979-VerfasserInautProf. Dr. Dr. h. c.PeterLangerAkademischeR BetreuerIndgsProf. Dr.SabineMüllerAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg[doi]10.18453/rosdok_id00000983[purl]http://purl.uni-rostock.de/rosdok/id00000983[urn]urn:nbn:de:gbv:28-diss2012-0018-7open_access20112011epoch:21th_centuryrfc5646:endoctype:epub.dissertationaccesscondition:openaccessSDNB:540institution:unirostock.mnfstate:published