mycoreobjectrosdok_disshab_0000000523rosdok_disshab_0000000523rosdokdisshabrosdok_derivate_00000044202023-08-08T10:02:07.359Z2010-11-22T12:07:03.759Zadministratorpublished1rosdok_derivate_0000004420truetruederivate_types:fulltextVolltextfulltextwf_edit_epub wf_register_epubstate:publishedstate:publishedveröffentlichtpublishedrosdok/id00000733640364160MODS updated during RosDok migration in June 2021DissertationHochschulschrift142870900AliAsad1982-VerfasserInautSynthesis of Sterically Encumbered Biaryls by [3+3] Cyclocondensation Reactions and Synthesis of Arylated Pyrazoles, Bis(diaryl)sulfones, and Bis(alkenyl)pyridines by Pd(0)-Catalysed Cross-Coupling ReactionsenProf. Dr.PeterLangerAkademischeR BetreuerIndgsProf. Dr.AndreasKirschningAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00000733http://purl.uni-rostock.de/rosdok/id00000733urn:nbn:de:gbv:28-diss2010-0156-3540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2010monographic20102010Universitätsbibliothek RostockRostock20102010Sterically encumbered biaryls were prepared [3+3] cyclocondensation. Arylatde pyrazoles, and bis(diaryl)sulfones were prepared by Suzuki-Miyuara reaction in very good yield.Di(alkenyl)pyridines and bipyridyls were prepared by Heck reaction.Bipyridyls were the unexpected products.bipyridinesbis triflatesdouble Heck couplingUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000733doctype: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 Sterically Encumbered Biaryls by [3+3] Cyclocondensation Reactions and Synthesis of Arylated Pyrazoles, Bis(diaryl)sulfones, and Bis(alkenyl)pyridines by Pd(0)-Catalysed Cross-Coupling ReactionsSynthesis of Sterically Encumbered Biaryls by [3+3] Cyclocondensation Reactions and Synthesis of Arylated Pyrazoles, Bis(diaryl)sulfones, and Bis(alkenyl)pyridines by Pd(0)-Catalysed Cross-Coupling Reactionsgnd:142870900gnd:2147083-2gnd:142870900gnd:2147083-2rosdok_disshab_0000000523-d717173e39gnd:142870900Ali AsadAli Asadrosdok_disshab_0000000523-d717173e60Prof. Dr. Peter LangerProf. Dr. Peter Langerrosdok_disshab_0000000523-d717173e72Prof. Dr. Andreas KirschningProf. Dr. Andreas Kirschningrosdok_disshab_0000000523-d717173e84gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätAli AsadProf. Dr. Peter LangerProf. Dr. Andreas KirschningUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätAli AsadProf. Dr. Peter LangerProf. Dr. Andreas KirschningUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätAli AsadRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00000733http://purl.uni-rostock.de/rosdok/id00000733urn:nbn:de:gbv:28-diss2010-0156-3bipyridinesbis triflatesdouble Heck couplingSterically encumbered biaryls were prepared [3+3] cyclocondensation. Arylatde pyrazoles, and bis(diaryl)sulfones were prepared by Suzuki-Miyuara reaction in very good yield.Di(alkenyl)pyridines and bipyridyls were prepared by Heck reaction.Bipyridyls were the unexpected products.20102010epub.dissertation1 Dissertation_Asad_2010.pdf 2123586 a1ca515f4e96003cc19afae6f9305552 rosdok/id00000733640364160MODS updated during RosDok migration in June 2021DissertationHochschulschrift142870900AliAsad1982-VerfasserInautSynthesis of Sterically Encumbered Biaryls by [3+3] Cyclocondensation Reactions and Synthesis of Arylated Pyrazoles, Bis(diaryl)sulfones, and Bis(alkenyl)pyridines by Pd(0)-Catalysed Cross-Coupling ReactionsenProf. Dr.PeterLangerAkademischeR BetreuerIndgsProf. Dr.AndreasKirschningAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00000733http://purl.uni-rostock.de/rosdok/id00000733urn:nbn:de:gbv:28-diss2010-0156-3540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2010monographic20102010Universitätsbibliothek RostockRostock20102010Sterically encumbered biaryls were prepared [3+3] cyclocondensation. Arylatde pyrazoles, and bis(diaryl)sulfones were prepared by Suzuki-Miyuara reaction in very good yield.Di(alkenyl)pyridines and bipyridyls were prepared by Heck reaction.Bipyridyls were the unexpected products.bipyridinesbis triflatesdouble Heck couplingUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000733 2010-11-22T12:07:03.759Z 2023-08-08T10:02:07.359Z 2023-08-18T10:02:07.364Z {"identifier":"rosdok/id00000733","type":"local_id","additional":"","service":"MCRLocalID","created":"2018-06-30T12:47:19.109Z"} {"identifier":"http://purl.uni-rostock.de/rosdok/id00000733","type":"purl","additional":"","service":"RosDokPURL","created":"2018-06-30T12:47:19.308Z","registered":"2018-06-30T12:47:19.308Z"} {"identifier":"10.18453/rosdok_id00000733","type":"doi","additional":"","service":"RosDokDOI","created":"2018-06-30T12:47:20.743Z","registered":"2018-06-30T12:47:20.743Z"} {"identifier":"urn:nbn:de:gbv:28-diss2010-0156-3","type":"dnbUrn","additional":"","service":"RosDokURN","created":"2018-06-30T12:47:19.114Z","registered":"2010-11-24T03:01:56.743Z"} administratorfulltextfile/rosdok_disshab_0000000523/rosdok_derivate_0000004420/Dissertation_Asad_2010.pdfSynthesis of Sterically Encumbered Biaryls by [3+3] Cyclocondensation Reactions and Synthesis of Arylated Pyrazoles, Bis(diaryl)sulfones, and Bis(alkenyl)pyridines by Pd(0)-Catalysed Cross-Coupling ReactionsSynthesis of Sterically Encumbered Biaryls by [3+3] Cyclocondensation Reactions and Synthesis of Arylated Pyrazoles, Bis(diaryl)sulfones, and Bis(alkenyl)pyridines by Pd(0)-Catalysed Cross-Coupling Reactionsgnd:142870900gnd:2147083-2gnd:142870900gnd:2147083-2rosdok_disshab_0000000523-d717173e39gnd:142870900Ali AsadAli Asadrosdok_disshab_0000000523-d717173e60Prof. Dr. Peter LangerProf. Dr. Peter Langerrosdok_disshab_0000000523-d717173e72Prof. Dr. Andreas KirschningProf. Dr. Andreas Kirschningrosdok_disshab_0000000523-d717173e84gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätAli AsadProf. Dr. Peter LangerProf. Dr. Andreas KirschningUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätAli AsadProf. Dr. Peter LangerProf. Dr. Andreas KirschningUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätAli AsadRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00000733http://purl.uni-rostock.de/rosdok/id00000733urn:nbn:de:gbv:28-diss2010-0156-3bipyridinesbis triflatesdouble Heck couplingSterically encumbered biaryls were prepared [3+3] cyclocondensation. Arylatde pyrazoles, and bis(diaryl)sulfones were prepared by Suzuki-Miyuara reaction in very good yield.Di(alkenyl)pyridines and bipyridyls were prepared by Heck reaction.Bipyridyls were the unexpected products.20102010[xslt]Saxonrosdok/id00000733https://purl.uni-rostock.de/rosdok/id0000073364036416010.18453/rosdok_id00000733urn:nbn:de:gbv:28-diss2010-0156-3Ali AsadAsad AliSynthesis of Sterically Encumbered Biaryls by [3+3] Cyclocondensation Reactions and Synthesis of Arylated Pyrazoles, Bis(diaryl)sulfones, and Bis(alkenyl)pyridines by Pd(0)-Catalysed Cross-Coupling ReactionsDissertationdoctoral thesisUniversität Rostock, 2010Sterically encumbered biaryls were prepared [3+3] cyclocondensation. Arylatde pyrazoles, and bis(diaryl)sulfones were prepared by Suzuki-Miyuara reaction in very good yield.Di(alkenyl)pyridines and bipyridyls were prepared by Heck reaction.Bipyridyls were the unexpected products.Ali AsadSynthesis of Sterically Encumbered Biaryls by [3+3] Cyclocondensation Reactions and Synthesis of Arylated Pyrazoles, Bis(diaryl)sulfones, and Bis(alkenyl)pyridines by Pd(0)-Catalysed Cross-Coupling ReactionsUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000733142870900AliAsad1982-VerfasserInautProf. Dr.PeterLangerAkademischeR BetreuerIndgsProf. Dr.AndreasKirschningAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg[doi]10.18453/rosdok_id00000733[purl]http://purl.uni-rostock.de/rosdok/id00000733[urn]urn:nbn:de:gbv:28-diss2010-0156-3open_access20102010epoch:21th_centuryrfc5646:endoctype:epub.dissertationaccesscondition:openaccessSDNB:540institution:unirostock.mnfstate:published