mycoreobjectrosdok_disshab_0000000675rosdok_disshab_0000000675rosdokdisshabrosdok_derivate_00000046502023-08-08T10:02:44.928Z2011-07-22T11:02:55.652Zadministratorpublished1rosdok_derivate_0000004650truetruederivate_types:fulltextVolltextfulltextwf_edit_epub wf_register_epubstate:publishedstate:publishedveröffentlichtpublishedrosdok/id0000087366467495XMODS updated during RosDok migration in June 2021DissertationHochschulschrift1013756142Thai HungNguyen1976-VerfasserInautNew Palladium(0)-Catalyzed Reactions of 2,3-Dibromobenzofuran, 2,3,5-Tribromobenzofuran, and 2,3-DibromoindenonedeProf. Dr.PeterLangeAkademischeR BetreuerIndgsProf. Dr.TillOpadtzAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00000873http://purl.uni-rostock.de/rosdok/id00000873urn:nbn:de:gbv:28-diss2011-0102-7540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2010monographic20112010Universitätsbibliothek RostockRostock20112011Functionalized dibenzofurans were prepared based on domino twofold Heck / 6-electrocyclization reactions of 2,3-di- and 2,3,5-tribromobenzofuran. The Suzuki–Miyaura reaction of 2,3-dibromobenzofuran with one equivalent of arylboronic acids resulted in site-selective. 2,3-Diarylbenzofurans containing two different aryl groups were prepared from in a one-pot protocol. The Suzuki-Miyaura reaction of 2,3-dibromo-1H-inden-1-one with one equivalent of arylboronic acid gave 2-bromo-3-aryl-1H-inden-1-ones with very good site-selectivity. The one-pot reaction also afforded 2,3-diaryl-1H-inden-1-ones containing two different terminal aryl groups.functionalized dibenzofuransregioselective arylationone-pot synthesisUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000873doctype: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:derfc5646:deDeutschGermangerdeuSDNB: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/New Palladium(0)-Catalyzed Reactions of 2,3-Dibromobenzofuran, 2,3,5-Tribromobenzofuran, and 2,3-DibromoindenoneNew Palladium(0)-Catalyzed Reactions of 2,3-Dibromobenzofuran, 2,3,5-Tribromobenzofuran, and 2,3-Dibromoindenonegnd:1013756142gnd:2147083-2gnd:1013756142gnd:2147083-2rosdok_disshab_0000000675-d4885815e39gnd:1013756142Thai Hung NguyenThai Hung Nguyenrosdok_disshab_0000000675-d4885815e60Prof. Dr. Peter LangeProf. Dr. Peter Langerosdok_disshab_0000000675-d4885815e72Prof. Dr. Till OpadtzProf. Dr. Till Opadtzrosdok_disshab_0000000675-d4885815e84gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätThai Hung NguyenProf. Dr. Peter LangeProf. Dr. Till OpadtzUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätThai Hung NguyenProf. Dr. Peter LangeProf. Dr. Till OpadtzUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätThai Hung NguyenRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00000873http://purl.uni-rostock.de/rosdok/id00000873urn:nbn:de:gbv:28-diss2011-0102-7functionalized dibenzofuransregioselective arylationone-pot synthesisFunctionalized dibenzofurans were prepared based on domino twofold Heck / 6-electrocyclization reactions of 2,3-di- and 2,3,5-tribromobenzofuran. The Suzuki–Miyaura reaction of 2,3-dibromobenzofuran with one equivalent of arylboronic acids resulted in site-selective. 2,3-Diarylbenzofurans containing two different aryl groups were prepared from in a one-pot protocol. The Suzuki-Miyaura reaction of 2,3-dibromo-1H-inden-1-one with one equivalent of arylboronic acid gave 2-bromo-3-aryl-1H-inden-1-ones with very good site-selectivity. The one-pot reaction also afforded 2,3-diaryl-1H-inden-1-ones containing two different terminal aryl groups.20102010epub.dissertation1 Dissertation_Nguyen_2011.pdf 1445793 1b28be6df8777d8928de29e526be26f5 rosdok/id0000087366467495XMODS updated during RosDok migration in June 2021DissertationHochschulschrift1013756142Thai HungNguyen1976-VerfasserInautNew Palladium(0)-Catalyzed Reactions of 2,3-Dibromobenzofuran, 2,3,5-Tribromobenzofuran, and 2,3-DibromoindenonedeProf. Dr.PeterLangeAkademischeR BetreuerIndgsProf. Dr.TillOpadtzAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00000873http://purl.uni-rostock.de/rosdok/id00000873urn:nbn:de:gbv:28-diss2011-0102-7540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2010monographic20112010Universitätsbibliothek RostockRostock20112011Functionalized dibenzofurans were prepared based on domino twofold Heck / 6-electrocyclization reactions of 2,3-di- and 2,3,5-tribromobenzofuran. The Suzuki–Miyaura reaction of 2,3-dibromobenzofuran with one equivalent of arylboronic acids resulted in site-selective. 2,3-Diarylbenzofurans containing two different aryl groups were prepared from in a one-pot protocol. The Suzuki-Miyaura reaction of 2,3-dibromo-1H-inden-1-one with one equivalent of arylboronic acid gave 2-bromo-3-aryl-1H-inden-1-ones with very good site-selectivity. 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The Suzuki–Miyaura reaction of 2,3-dibromobenzofuran with one equivalent of arylboronic acids resulted in site-selective. 2,3-Diarylbenzofurans containing two different aryl groups were prepared from in a one-pot protocol. The Suzuki-Miyaura reaction of 2,3-dibromo-1H-inden-1-one with one equivalent of arylboronic acid gave 2-bromo-3-aryl-1H-inden-1-ones with very good site-selectivity. The one-pot reaction also afforded 2,3-diaryl-1H-inden-1-ones containing two different terminal aryl groups.20102010[xslt]Saxonrosdok/id00000873https://purl.uni-rostock.de/rosdok/id0000087366467495X10.18453/rosdok_id00000873urn:nbn:de:gbv:28-diss2011-0102-7Thai Hung NguyenNguyen Thai HungNew Palladium(0)-Catalyzed Reactions of 2,3-Dibromobenzofuran, 2,3,5-Tribromobenzofuran, and 2,3-DibromoindenoneDissertationdoctoral thesisUniversität Rostock, 2010Functionalized dibenzofurans were prepared based on domino twofold Heck / 6-electrocyclization reactions of 2,3-di- and 2,3,5-tribromobenzofuran. The Suzuki–Miyaura reaction of 2,3-dibromobenzofuran with one equivalent of arylboronic acids resulted in site-selective. 2,3-Diarylbenzofurans containing…Thai Hung NguyenNew Palladium(0)-Catalyzed Reactions of 2,3-Dibromobenzofuran, 2,3,5-Tribromobenzofuran, and 2,3-DibromoindenoneUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id000008731013756142Thai HungNguyen1976-VerfasserInautProf. Dr.PeterLangeAkademischeR BetreuerIndgsProf. Dr.TillOpadtzAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg[doi]10.18453/rosdok_id00000873[purl]http://purl.uni-rostock.de/rosdok/id00000873[urn]urn:nbn:de:gbv:28-diss2011-0102-7open_access20102010epoch:21th_centuryrfc5646:dedoctype:epub.dissertationaccesscondition:openaccessSDNB:540institution:unirostock.mnfstate:published