mycoreobjectrosdok_disshab_0000000530rosdok_disshab_0000000530rosdokdisshabrosdok_derivate_00000044312023-08-08T10:02:08.540Z2010-11-24T14:17:54.234Zadministratorpublished1rosdok_derivate_0000004431truetruederivate_types:fulltextVolltextfulltextwf_edit_epub wf_register_epubstate:publishedstate:publishedveröffentlichtpublishedrosdok/id00000739640480357MODS updated during RosDok migration in June 2021DissertationHochschulschrift14287082XRasheed AhmadKhera1980-VerfasserInautSynthesis of Functionalized Triarylmethanes and Pyranones Based on Cyclization Reactions of Free and Masked Dianions and Regioselective Palladium(0)-Catalyzed Reactions of Functionalized Sulfones, Benzophenones, Pyrazoles, Indenones, and FuransenProf. Dr.PeterLangerAkademischeR BetreuerIndgsProf. Dr.MartinKöckerlingAkademischeR BetreuerIndgsProf. Dr.PeterMetzAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00000739http://purl.uni-rostock.de/rosdok/id00000739urn:nbn:de:gbv:28-diss2010-0163-2540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2010monographic20102010Universitätsbibliothek RostockRostock20102010Functionalized triarylmethanes were prepared with [3+3] cyclization. 2,3-dihydro fluorinated and non fluorinated pyranones were prepared in one step strategy. The Regioselective Suzuki-Miyaura and Sonogashira reaction of the bis(triflates) of 2,4-dihydroxybenzophenone and ,2,4-dihydroxydiphenylsulfone and 2,3-Dibromoindenone with arylboronic acids gave 2,4-diarylbenzophenones and 2,3-dibromoindenone were also studied. Furthermore, The Suzuki-Miyaura reactions of N-protected 3,4,5-tribromopyrazole, 2,3,4,5-tetrabromofuran.Funktionalisierte Triarylmethane wurden durch [3+3]-Cyclisierungen dargestellt. Fluorierte 2,3-Dihydro- und nicht fluorierte pyranone wurden in einem Schritt. Regioselektive Suzuki-Miyaura- und Sonogashira-Reaktionen der Bistriflate des 2,4-Dihydroxybenzophenons und des 2,4′-Dihydroxydiphenylsulfones und 2,3-Dibromindenone. Die Suzuki-Miyaura-Reaktionen von N-geschützten 3,4,5-Tribrompyrazolen, 2,3,4,5-Tetrabromfuranen.Suzuki reactionSonogashira reactionmetal catalyzed reactionUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000739doctype: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 Triarylmethanes and Pyranones Based on Cyclization Reactions of Free and Masked Dianions and Regioselective Palladium(0)-Catalyzed Reactions of Functionalized Sulfones, Benzophenones, Pyrazoles, Indenones, and FuransSynthesis of Functionalized Triarylmethanes and Pyranones Based on Cyclization Reactions of Free and Masked Dianions and Regioselective Palladium(0)-Catalyzed Reactions of Functionalized Sulfones, Benzophenones, Pyrazoles, Indenones, and Furansgnd:14287082Xgnd:2147083-2gnd:14287082Xgnd:2147083-2rosdok_disshab_0000000530-d1692527e39gnd:14287082XRasheed Ahmad KheraRasheed Ahmad Kherarosdok_disshab_0000000530-d1692527e60Prof. Dr. Peter LangerProf. Dr. Peter Langerrosdok_disshab_0000000530-d1692527e72Prof. Dr. Martin KöckerlingProf. Dr. Martin Köckerlingrosdok_disshab_0000000530-d1692527e84Prof. Dr. Peter MetzProf. Dr. Peter Metzrosdok_disshab_0000000530-d1692527e97gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätRasheed Ahmad KheraProf. Dr. Peter LangerProf. Dr. Martin KöckerlingProf. Dr. Peter MetzUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätRasheed Ahmad KheraProf. Dr. Peter LangerProf. Dr. Martin KöckerlingProf. Dr. Peter MetzUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätRasheed Ahmad KheraRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00000739http://purl.uni-rostock.de/rosdok/id00000739urn:nbn:de:gbv:28-diss2010-0163-2Suzuki reactionSonogashira reactionmetal catalyzed reactionFunctionalized triarylmethanes were prepared with [3+3] cyclization. 2,3-dihydro fluorinated and non fluorinated pyranones were prepared in one step strategy. The Regioselective Suzuki-Miyaura and Sonogashira reaction of the bis(triflates) of 2,4-dihydroxybenzophenone and ,2,4-dihydroxydiphenylsulfone and 2,3-Dibromoindenone with arylboronic acids gave 2,4-diarylbenzophenones and 2,3-dibromoindenone were also studied. Furthermore, The Suzuki-Miyaura reactions of N-protected 3,4,5-tribromopyrazole, 2,3,4,5-tetrabromofuran.Funktionalisierte Triarylmethane wurden durch [3+3]-Cyclisierungen dargestellt. Fluorierte 2,3-Dihydro- und nicht fluorierte pyranone wurden in einem Schritt. Regioselektive Suzuki-Miyaura- und Sonogashira-Reaktionen der Bistriflate des 2,4-Dihydroxybenzophenons und des 2,4′-Dihydroxydiphenylsulfones und 2,3-Dibromindenone. Die Suzuki-Miyaura-Reaktionen von N-geschützten 3,4,5-Tribrompyrazolen, 2,3,4,5-Tetrabromfuranen.20102010epub.dissertation1 Dissertation_Khera_2010.pdf 2208507 2b65213b5c262d0be4cfbb2db6d1671d rosdok/id00000739640480357MODS updated during RosDok migration in June 2021DissertationHochschulschrift14287082XRasheed AhmadKhera1980-VerfasserInautSynthesis of Functionalized Triarylmethanes and Pyranones Based on Cyclization Reactions of Free and Masked Dianions and Regioselective Palladium(0)-Catalyzed Reactions of Functionalized Sulfones, Benzophenones, Pyrazoles, Indenones, and FuransenProf. Dr.PeterLangerAkademischeR BetreuerIndgsProf. Dr.MartinKöckerlingAkademischeR BetreuerIndgsProf. Dr.PeterMetzAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00000739http://purl.uni-rostock.de/rosdok/id00000739urn:nbn:de:gbv:28-diss2010-0163-2540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2010monographic20102010Universitätsbibliothek RostockRostock20102010Functionalized triarylmethanes were prepared with [3+3] cyclization. 2,3-dihydro fluorinated and non fluorinated pyranones were prepared in one step strategy. The Regioselective Suzuki-Miyaura and Sonogashira reaction of the bis(triflates) of 2,4-dihydroxybenzophenone and ,2,4-dihydroxydiphenylsulfone and 2,3-Dibromoindenone with arylboronic acids gave 2,4-diarylbenzophenones and 2,3-dibromoindenone were also studied. Furthermore, The Suzuki-Miyaura reactions of N-protected 3,4,5-tribromopyrazole, 2,3,4,5-tetrabromofuran.Funktionalisierte Triarylmethane wurden durch [3+3]-Cyclisierungen dargestellt. Fluorierte 2,3-Dihydro- und nicht fluorierte pyranone wurden in einem Schritt. Regioselektive Suzuki-Miyaura- und Sonogashira-Reaktionen der Bistriflate des 2,4-Dihydroxybenzophenons und des 2,4′-Dihydroxydiphenylsulfones und 2,3-Dibromindenone. Die Suzuki-Miyaura-Reaktionen von N-geschützten 3,4,5-Tribrompyrazolen, 2,3,4,5-Tetrabromfuranen.Suzuki reactionSonogashira reactionmetal catalyzed reactionUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00000739 2010-11-24T14:17:54.234Z 2023-08-08T10:02:08.540Z 2023-08-18T10:02:08.545Z {"identifier":"rosdok/id00000739","type":"local_id","additional":"","service":"MCRLocalID","created":"2018-06-30T12:47:33.287Z"} {"identifier":"http://purl.uni-rostock.de/rosdok/id00000739","type":"purl","additional":"","service":"RosDokPURL","created":"2018-06-30T12:47:33.474Z","registered":"2018-06-30T12:47:33.474Z"} {"identifier":"10.18453/rosdok_id00000739","type":"doi","additional":"","service":"RosDokDOI","created":"2018-06-30T12:47:34.758Z","registered":"2018-06-30T12:47:34.758Z"} {"identifier":"urn:nbn:de:gbv:28-diss2010-0163-2","type":"dnbUrn","additional":"","service":"RosDokURN","created":"2018-06-30T12:47:33.292Z","registered":"2010-11-25T03:01:49.393Z"} administratorfulltextfile/rosdok_disshab_0000000530/rosdok_derivate_0000004431/Dissertation_Khera_2010.pdfSynthesis of Functionalized Triarylmethanes and Pyranones Based on Cyclization Reactions of Free and Masked Dianions and Regioselective Palladium(0)-Catalyzed Reactions of Functionalized Sulfones, Benzophenones, Pyrazoles, Indenones, and FuransSynthesis of Functionalized Triarylmethanes and Pyranones Based on Cyclization Reactions of Free and Masked Dianions and Regioselective Palladium(0)-Catalyzed Reactions of Functionalized Sulfones, Benzophenones, Pyrazoles, Indenones, and Furansgnd:14287082Xgnd:2147083-2gnd:14287082Xgnd:2147083-2rosdok_disshab_0000000530-d1692527e39gnd:14287082XRasheed Ahmad KheraRasheed Ahmad Kherarosdok_disshab_0000000530-d1692527e60Prof. Dr. Peter LangerProf. Dr. Peter Langerrosdok_disshab_0000000530-d1692527e72Prof. Dr. Martin KöckerlingProf. Dr. Martin Köckerlingrosdok_disshab_0000000530-d1692527e84Prof. Dr. Peter MetzProf. Dr. Peter Metzrosdok_disshab_0000000530-d1692527e97gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätRasheed Ahmad KheraProf. Dr. Peter LangerProf. Dr. Martin KöckerlingProf. Dr. Peter MetzUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätRasheed Ahmad KheraProf. Dr. Peter LangerProf. Dr. Martin KöckerlingProf. Dr. Peter MetzUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätRasheed Ahmad KheraRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00000739http://purl.uni-rostock.de/rosdok/id00000739urn:nbn:de:gbv:28-diss2010-0163-2Suzuki reactionSonogashira reactionmetal catalyzed reactionFunctionalized triarylmethanes were prepared with [3+3] cyclization. 2,3-dihydro fluorinated and non fluorinated pyranones were prepared in one step strategy. The Regioselective Suzuki-Miyaura and Sonogashira reaction of the bis(triflates) of 2,4-dihydroxybenzophenone and ,2,4-dihydroxydiphenylsulfone and 2,3-Dibromoindenone with arylboronic acids gave 2,4-diarylbenzophenones and 2,3-dibromoindenone were also studied. Furthermore, The Suzuki-Miyaura reactions of N-protected 3,4,5-tribromopyrazole, 2,3,4,5-tetrabromofuran.Funktionalisierte Triarylmethane wurden durch [3+3]-Cyclisierungen dargestellt. Fluorierte 2,3-Dihydro- und nicht fluorierte pyranone wurden in einem Schritt. Regioselektive Suzuki-Miyaura- und Sonogashira-Reaktionen der Bistriflate des 2,4-Dihydroxybenzophenons und des 2,4′-Dihydroxydiphenylsulfones und 2,3-Dibromindenone. Die Suzuki-Miyaura-Reaktionen von N-geschützten 3,4,5-Tribrompyrazolen, 2,3,4,5-Tetrabromfuranen.20102010[xslt]Saxonrosdok/id00000739https://purl.uni-rostock.de/rosdok/id0000073964048035710.18453/rosdok_id00000739urn:nbn:de:gbv:28-diss2010-0163-2Rasheed Ahmad KheraKhera Rasheed AhmadSynthesis of Functionalized Triarylmethanes and Pyranones Based on Cyclization Reactions of Free and Masked Dianions and Regioselective Palladium(0)-Catalyzed Reactions of Functionalized Sulfones, Benzophenones, Pyrazoles, Indenones, and FuransDissertationdoctoral thesisUniversität Rostock, 2010Functionalized triarylmethanes were prepared with [3+3] cyclization. 2,3-dihydro fluorinated and non fluorinated pyranones were prepared in one step strategy. The Regioselective Suzuki-Miyaura and Sonogashira reaction of the bis(triflates) of 2,4-dihydroxybenzophenone and…Rasheed Ahmad KheraSynthesis of Functionalized Triarylmethanes and Pyranones Based on Cyclization Reactions of Free and Masked Dianions and Regioselective Palladium(0)-Catalyzed Reactions of Functionalized Sulfones, Benzophenones, Pyrazoles, Indenones, and FuransUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id0000073914287082XRasheed AhmadKhera1980-VerfasserInautProf. Dr.PeterLangerAkademischeR BetreuerIndgsProf. Dr.MartinKöckerlingAkademischeR BetreuerIndgsProf. Dr.PeterMetzAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg[doi]10.18453/rosdok_id00000739[purl]http://purl.uni-rostock.de/rosdok/id00000739[urn]urn:nbn:de:gbv:28-diss2010-0163-2open_access20102010epoch:21th_centuryrfc5646:endoctype:epub.dissertationaccesscondition:openaccessSDNB:540institution:unirostock.mnfstate:published