mycoreobjectrosdok_disshab_0000000594rosdok_disshab_0000000594rosdokdisshabrosdok_derivate_00000045632023-08-08T10:02:25.258Z2011-01-25T08:14:09.068Zadministratorpublished1rosdok_derivate_0000004563truetruederivate_types:fulltextVolltextfulltextwf_edit_epub wf_register_epubstate:publishedstate:publishedveröffentlichtpublishedrosdok/id00000798647077450MODS updated during RosDok migration in June 2021DissertationHochschulschrift143545175MunawarHussain1977-VerfasserInautDomino Twofold Heck / 6p-Electrocyclization and Regioselective Palladium(0)-Catalyzed Reactions of Brominated Indoles, Furans, Naphthoquinone and 2,4,5,6-TetrachloropyrimidineenProf. Dr.PeterLangerAkademischeR BetreuerIndgsProf. Dr.ScottTaylorAkademischeR BetreuerIndgsProf. Dr.WilliKantlehnerAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00000798http://purl.uni-rostock.de/rosdok/id00000798urn:nbn:de:gbv:28-diss2011-0021-7540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2010monographic20112010Universitätsbibliothek RostockRostock20112011I have synthesized functionalized carbazoles and benzofurans based on domino twofold Heck / 6pi-electrocyclization reactions. Functionalized anthraquinones, fluorenones and benzocoumarines were also prepared by this methodology. Regioselctive Suzuki-Miyaura cross-coupling reactions of 2,4,5,6-tetrachloropyrimidine and 2,3,4,5-tetrabromofuran provided an expedient synthesis of mono-, di-, tri- and tetraaryl-pyrimidines and di- and tetraarylfurans.domino twofold heckelectrocyclizationSuzuki reactionscatalysisUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000798doctype: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/Domino Twofold Heck / 6p-Electrocyclization and Regioselective Palladium(0)-Catalyzed Reactions of Brominated Indoles, Furans, Naphthoquinone and 2,4,5,6-TetrachloropyrimidineDomino Twofold Heck / 6p-Electrocyclization and Regioselective Palladium(0)-Catalyzed Reactions of Brominated Indoles, Furans, Naphthoquinone and 2,4,5,6-Tetrachloropyrimidinegnd:143545175gnd:2147083-2gnd:143545175gnd:2147083-2rosdok_disshab_0000000594-d1054377e39gnd:143545175Munawar HussainMunawar Hussainrosdok_disshab_0000000594-d1054377e60Prof. Dr. Peter LangerProf. Dr. Peter Langerrosdok_disshab_0000000594-d1054377e72Prof. Dr. Scott TaylorProf. Dr. Scott Taylorrosdok_disshab_0000000594-d1054377e84Prof. Dr. Willi KantlehnerProf. Dr. Willi Kantlehnerrosdok_disshab_0000000594-d1054377e97gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätMunawar HussainProf. Dr. Peter LangerProf. Dr. Scott TaylorProf. Dr. Willi KantlehnerUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätMunawar HussainProf. Dr. Peter LangerProf. Dr. Scott TaylorProf. Dr. Willi KantlehnerUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätMunawar HussainRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00000798http://purl.uni-rostock.de/rosdok/id00000798urn:nbn:de:gbv:28-diss2011-0021-7domino twofold heckelectrocyclizationSuzuki reactionscatalysisI have synthesized functionalized carbazoles and benzofurans based on domino twofold Heck / 6pi-electrocyclization reactions. Functionalized anthraquinones, fluorenones and benzocoumarines were also prepared by this methodology. Regioselctive Suzuki-Miyaura cross-coupling reactions of 2,4,5,6-tetrachloropyrimidine and 2,3,4,5-tetrabromofuran provided an expedient synthesis of mono-, di-, tri- and tetraaryl-pyrimidines and di- and tetraarylfurans.20102010epub.dissertation1 Dissertation_Hussain_2011.pdf 1724330 6f1d55aac6c8365e720260ee77e44823 rosdok/id00000798647077450MODS updated during RosDok migration in June 2021DissertationHochschulschrift143545175MunawarHussain1977-VerfasserInautDomino Twofold Heck / 6p-Electrocyclization and Regioselective Palladium(0)-Catalyzed Reactions of Brominated Indoles, Furans, Naphthoquinone and 2,4,5,6-TetrachloropyrimidineenProf. Dr.PeterLangerAkademischeR BetreuerIndgsProf. Dr.ScottTaylorAkademischeR BetreuerIndgsProf. Dr.WilliKantlehnerAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00000798http://purl.uni-rostock.de/rosdok/id00000798urn:nbn:de:gbv:28-diss2011-0021-7540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2010monographic20112010Universitätsbibliothek RostockRostock20112011I have synthesized functionalized carbazoles and benzofurans based on domino twofold Heck / 6pi-electrocyclization reactions. Functionalized anthraquinones, fluorenones and benzocoumarines were also prepared by this methodology. Regioselctive Suzuki-Miyaura cross-coupling reactions of 2,4,5,6-tetrachloropyrimidine and 2,3,4,5-tetrabromofuran provided an expedient synthesis of mono-, di-, tri- and tetraaryl-pyrimidines and di- and tetraarylfurans.domino twofold heckelectrocyclizationSuzuki reactionscatalysisUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000798 2011-01-25T08:14:09.068Z 2023-08-08T10:02:25.258Z 2023-08-18T10:02:25.263Z {"identifier":"rosdok/id00000798","type":"local_id","additional":"","service":"MCRLocalID","created":"2018-06-30T12:49:43.287Z"} {"identifier":"http://purl.uni-rostock.de/rosdok/id00000798","type":"purl","additional":"","service":"RosDokPURL","created":"2018-06-30T12:49:43.479Z","registered":"2018-06-30T12:49:43.479Z"} {"identifier":"10.18453/rosdok_id00000798","type":"doi","additional":"","service":"RosDokDOI","created":"2018-06-30T12:49:44.763Z","registered":"2018-06-30T12:49:44.763Z"} {"identifier":"urn:nbn:de:gbv:28-diss2011-0021-7","type":"dnbUrn","additional":"","service":"RosDokURN","created":"2018-06-30T12:49:43.293Z","registered":"2011-02-19T03:21:26.207Z"} administratorfulltextfile/rosdok_disshab_0000000594/rosdok_derivate_0000004563/Dissertation_Hussain_2011.pdfDomino Twofold Heck / 6p-Electrocyclization and Regioselective Palladium(0)-Catalyzed Reactions of Brominated Indoles, Furans, Naphthoquinone and 2,4,5,6-TetrachloropyrimidineDomino Twofold Heck / 6p-Electrocyclization and Regioselective Palladium(0)-Catalyzed Reactions of Brominated Indoles, Furans, Naphthoquinone and 2,4,5,6-Tetrachloropyrimidinegnd:143545175gnd:2147083-2gnd:143545175gnd:2147083-2rosdok_disshab_0000000594-d1054377e39gnd:143545175Munawar HussainMunawar Hussainrosdok_disshab_0000000594-d1054377e60Prof. Dr. Peter LangerProf. Dr. Peter Langerrosdok_disshab_0000000594-d1054377e72Prof. Dr. Scott TaylorProf. Dr. Scott Taylorrosdok_disshab_0000000594-d1054377e84Prof. Dr. Willi KantlehnerProf. Dr. Willi Kantlehnerrosdok_disshab_0000000594-d1054377e97gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätMunawar HussainProf. Dr. Peter LangerProf. Dr. Scott TaylorProf. Dr. Willi KantlehnerUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätMunawar HussainProf. Dr. Peter LangerProf. Dr. Scott TaylorProf. Dr. Willi KantlehnerUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätMunawar HussainRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00000798http://purl.uni-rostock.de/rosdok/id00000798urn:nbn:de:gbv:28-diss2011-0021-7domino twofold heckelectrocyclizationSuzuki reactionscatalysisI have synthesized functionalized carbazoles and benzofurans based on domino twofold Heck / 6pi-electrocyclization reactions. Functionalized anthraquinones, fluorenones and benzocoumarines were also prepared by this methodology. Regioselctive Suzuki-Miyaura cross-coupling reactions of 2,4,5,6-tetrachloropyrimidine and 2,3,4,5-tetrabromofuran provided an expedient synthesis of mono-, di-, tri- and tetraaryl-pyrimidines and di- and tetraarylfurans.20102010[xslt]Saxonrosdok/id00000798https://purl.uni-rostock.de/rosdok/id0000079864707745010.18453/rosdok_id00000798urn:nbn:de:gbv:28-diss2011-0021-7Munawar HussainHussain MunawarDomino Twofold Heck / 6p-Electrocyclization and Regioselective Palladium(0)-Catalyzed Reactions of Brominated Indoles, Furans, Naphthoquinone and 2,4,5,6-TetrachloropyrimidineDissertationdoctoral thesisUniversität Rostock, 2010I have synthesized functionalized carbazoles and benzofurans based on domino twofold Heck / 6pi-electrocyclization reactions. Functionalized anthraquinones, fluorenones and benzocoumarines were also prepared by this methodology. Regioselctive Suzuki-Miyaura cross-coupling reactions of…Munawar HussainDomino Twofold Heck / 6p-Electrocyclization and Regioselective Palladium(0)-Catalyzed Reactions of Brominated Indoles, Furans, Naphthoquinone and 2,4,5,6-TetrachloropyrimidineUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000798143545175MunawarHussain1977-VerfasserInautProf. Dr.PeterLangerAkademischeR BetreuerIndgsProf. Dr.ScottTaylorAkademischeR BetreuerIndgsProf. Dr.WilliKantlehnerAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg[doi]10.18453/rosdok_id00000798[purl]http://purl.uni-rostock.de/rosdok/id00000798[urn]urn:nbn:de:gbv:28-diss2011-0021-7open_access20102010epoch:21th_centuryrfc5646:endoctype:epub.dissertationaccesscondition:openaccessSDNB:540institution:unirostock.mnfstate:published