mycoreobjectrosdok_disshab_0000000945rosdok_disshab_0000000945rosdokdisshabrosdok_derivate_00000050202023-08-08T10:03:54.993Z2013-03-19T12:55:31.950Zadministratorpublished1rosdok_derivate_0000005020truetruederivate_types:fulltextVolltextfulltextwf_edit_epub wf_register_epubstate:publishedstate:publishedveröffentlichtpublishedrosdok/id00001124739679139MODS updated during RosDok migration in June 2021DissertationHochschulschrift1032367652Muhammad FarooqIbad1982-VerfasserInautSynthesis of Highly Functionalized Carbacycles, Heterocycles and Silylium-Arene Adducts by Cyclocondensations, Palladium Catalyzed Cross-Coupling Reactions and Activation by Silylium CationenProf. Dr. Dr. h. c.PeterLangerAkademischeR BetreuerIndgsProf. Dr.AxelSchulzAkademischeR BetreuerIndgsProf. Dr.ManfredBraunAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00001124http://purl.uni-rostock.de/rosdok/id00001124urn:nbn:de:gbv:28-diss2013-0037-7540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2012monographic20122012Universitätsbibliothek RostockRostock20132013The Me3SiOTf-mediated condensation of 1-ethoxy-2-fluoro-1,3-bis trimethylsilyloxy) 1,3-dienes with 3-cyanochromones afforded fluorinated azaxanthones or biaryls. The [4+2] cycloaddition of 1-ethoxy-2-fluoro-1,3-bis(trimethylsilyloxy)-1,3-diene with DMAD afforded dimethyl 4-fluoro-3,5-dihydroxyphthalate. Various arylated phthalates, naphthoates, indoles, are synthesized Pd(0)-catalyzed Suzuki cross-coupling reaction and studied. The experimental and theoretical study of the silylium arene adducts ([Me3Si-Ar][B(C6F5)4]) and the catalytic trimerisation of bissilylated diazomethane are studied.silyliumwakly coordinating anionsdomino reactionsSzuki couplingDels alder reactiontrimerizationUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00001124doctype: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 Highly Functionalized Carbacycles, Heterocycles and Silylium-Arene Adducts by Cyclocondensations, Palladium Catalyzed Cross-Coupling Reactions and Activation by Silylium CationSynthesis of Highly Functionalized Carbacycles, Heterocycles and Silylium-Arene Adducts by Cyclocondensations, Palladium Catalyzed Cross-Coupling Reactions and Activation by Silylium Cationgnd:1032367652gnd:2147083-2gnd:1032367652gnd:2147083-2rosdok_disshab_0000000945-d560006e39gnd:1032367652Muhammad Farooq IbadMuhammad Farooq Ibadrosdok_disshab_0000000945-d560006e60Prof. Dr. Dr. h. c. Peter LangerProf. Dr. Dr. h. c. Peter Langerrosdok_disshab_0000000945-d560006e72Prof. Dr. Axel SchulzProf. Dr. Axel Schulzrosdok_disshab_0000000945-d560006e84Prof. Dr. Manfred BraunProf. Dr. Manfred Braunrosdok_disshab_0000000945-d560006e97gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätMuhammad Farooq IbadProf. Dr. Dr. h. c. Peter LangerProf. Dr. Axel SchulzProf. Dr. Manfred BraunUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätMuhammad Farooq IbadProf. Dr. Dr. h. c. Peter LangerProf. Dr. Axel SchulzProf. Dr. Manfred BraunUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätMuhammad Farooq IbadRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00001124http://purl.uni-rostock.de/rosdok/id00001124urn:nbn:de:gbv:28-diss2013-0037-7silyliumwakly coordinating anionsdomino reactionsSzuki couplingDels alder reactiontrimerizationThe Me3SiOTf-mediated condensation of 1-ethoxy-2-fluoro-1,3-bis trimethylsilyloxy) 1,3-dienes with 3-cyanochromones afforded fluorinated azaxanthones or biaryls. The [4+2] cycloaddition of 1-ethoxy-2-fluoro-1,3-bis(trimethylsilyloxy)-1,3-diene with DMAD afforded dimethyl 4-fluoro-3,5-dihydroxyphthalate. Various arylated phthalates, naphthoates, indoles, are synthesized Pd(0)-catalyzed Suzuki cross-coupling reaction and studied. The experimental and theoretical study of the silylium arene adducts ([Me3Si-Ar][B(C6F5)4]) and the catalytic trimerisation of bissilylated diazomethane are studied.20122012epub.dissertation1 Dissertation_Ibad_2013.pdf 4899809 2684957b25111b5437569aadd032e13d rosdok/id00001124739679139MODS updated during RosDok migration in June 2021DissertationHochschulschrift1032367652Muhammad FarooqIbad1982-VerfasserInautSynthesis of Highly Functionalized Carbacycles, Heterocycles and Silylium-Arene Adducts by Cyclocondensations, Palladium Catalyzed Cross-Coupling Reactions and Activation by Silylium CationenProf. Dr. Dr. h. c.PeterLangerAkademischeR BetreuerIndgsProf. Dr.AxelSchulzAkademischeR BetreuerIndgsProf. Dr.ManfredBraunAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00001124http://purl.uni-rostock.de/rosdok/id00001124urn:nbn:de:gbv:28-diss2013-0037-7540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2012monographic20122012Universitätsbibliothek RostockRostock20132013The Me3SiOTf-mediated condensation of 1-ethoxy-2-fluoro-1,3-bis trimethylsilyloxy) 1,3-dienes with 3-cyanochromones afforded fluorinated azaxanthones or biaryls. The [4+2] cycloaddition of 1-ethoxy-2-fluoro-1,3-bis(trimethylsilyloxy)-1,3-diene with DMAD afforded dimethyl 4-fluoro-3,5-dihydroxyphthalate. Various arylated phthalates, naphthoates, indoles, are synthesized Pd(0)-catalyzed Suzuki cross-coupling reaction and studied. The experimental and theoretical study of the silylium arene adducts ([Me3Si-Ar][B(C6F5)4]) and the catalytic trimerisation of bissilylated diazomethane are studied.silyliumwakly coordinating anionsdomino reactionsSzuki couplingDels alder reactiontrimerizationUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00001124 2013-03-19T12:55:31.950Z 2023-08-08T10:03:54.993Z 2023-08-18T10:03:54.998Z {"identifier":"rosdok/id00001124","type":"local_id","additional":"","service":"MCRLocalID","created":"2018-06-30T13:01:25.269Z"} {"identifier":"http://purl.uni-rostock.de/rosdok/id00001124","type":"purl","additional":"","service":"RosDokPURL","created":"2018-06-30T13:01:25.469Z","registered":"2018-06-30T13:01:25.469Z"} {"identifier":"10.18453/rosdok_id00001124","type":"doi","additional":"","service":"RosDokDOI","created":"2018-06-30T13:01:26.753Z","registered":"2018-06-30T13:01:26.753Z"} {"identifier":"urn:nbn:de:gbv:28-diss2013-0037-7","type":"dnbUrn","additional":"","service":"RosDokURN","created":"2018-06-30T13:01:25.274Z","registered":"2013-03-26T03:25:33.410Z"} administratorfulltextfile/rosdok_disshab_0000000945/rosdok_derivate_0000005020/Dissertation_Ibad_2013.pdfSynthesis of Highly Functionalized Carbacycles, Heterocycles and Silylium-Arene Adducts by Cyclocondensations, Palladium Catalyzed Cross-Coupling Reactions and Activation by Silylium CationSynthesis of Highly Functionalized Carbacycles, Heterocycles and Silylium-Arene Adducts by Cyclocondensations, Palladium Catalyzed Cross-Coupling Reactions and Activation by Silylium Cationgnd:1032367652gnd:2147083-2gnd:1032367652gnd:2147083-2rosdok_disshab_0000000945-d560006e39gnd:1032367652Muhammad Farooq IbadMuhammad Farooq Ibadrosdok_disshab_0000000945-d560006e60Prof. Dr. Dr. h. c. Peter LangerProf. Dr. Dr. h. c. Peter Langerrosdok_disshab_0000000945-d560006e72Prof. Dr. Axel SchulzProf. Dr. Axel Schulzrosdok_disshab_0000000945-d560006e84Prof. Dr. Manfred BraunProf. Dr. Manfred Braunrosdok_disshab_0000000945-d560006e97gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätMuhammad Farooq IbadProf. Dr. Dr. h. c. Peter LangerProf. Dr. Axel SchulzProf. Dr. Manfred BraunUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätMuhammad Farooq IbadProf. Dr. Dr. h. c. Peter LangerProf. Dr. Axel SchulzProf. Dr. Manfred BraunUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätMuhammad Farooq IbadRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00001124http://purl.uni-rostock.de/rosdok/id00001124urn:nbn:de:gbv:28-diss2013-0037-7silyliumwakly coordinating anionsdomino reactionsSzuki couplingDels alder reactiontrimerizationThe Me3SiOTf-mediated condensation of 1-ethoxy-2-fluoro-1,3-bis trimethylsilyloxy) 1,3-dienes with 3-cyanochromones afforded fluorinated azaxanthones or biaryls. The [4+2] cycloaddition of 1-ethoxy-2-fluoro-1,3-bis(trimethylsilyloxy)-1,3-diene with DMAD afforded dimethyl 4-fluoro-3,5-dihydroxyphthalate. Various arylated phthalates, naphthoates, indoles, are synthesized Pd(0)-catalyzed Suzuki cross-coupling reaction and studied. The experimental and theoretical study of the silylium arene adducts ([Me3Si-Ar][B(C6F5)4]) and the catalytic trimerisation of bissilylated diazomethane are studied.20122012[xslt]Saxonrosdok/id00001124https://purl.uni-rostock.de/rosdok/id0000112473967913910.18453/rosdok_id00001124urn:nbn:de:gbv:28-diss2013-0037-7Muhammad Farooq IbadIbad Muhammad FarooqSynthesis of Highly Functionalized Carbacycles, Heterocycles and Silylium-Arene Adducts by Cyclocondensations, Palladium Catalyzed Cross-Coupling Reactions and Activation by Silylium CationDissertationdoctoral thesisUniversität Rostock, 2012The Me3SiOTf-mediated condensation of 1-ethoxy-2-fluoro-1,3-bis trimethylsilyloxy) 1,3-dienes with 3-cyanochromones afforded fluorinated azaxanthones or biaryls. The [4+2] cycloaddition of 1-ethoxy-2-fluoro-1,3-bis(trimethylsilyloxy)-1,3-diene with DMAD afforded dimethyl…Muhammad Farooq IbadSynthesis of Highly Functionalized Carbacycles, Heterocycles and Silylium-Arene Adducts by Cyclocondensations, Palladium Catalyzed Cross-Coupling Reactions and Activation by Silylium CationUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id000011241032367652Muhammad FarooqIbad1982-VerfasserInautProf. Dr. Dr. h. c.PeterLangerAkademischeR BetreuerIndgsProf. Dr.AxelSchulzAkademischeR BetreuerIndgsProf. Dr.ManfredBraunAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg[doi]10.18453/rosdok_id00001124[purl]http://purl.uni-rostock.de/rosdok/id00001124[urn]urn:nbn:de:gbv:28-diss2013-0037-7open_access20122012epoch:21th_centuryrfc5646:endoctype:epub.dissertationaccesscondition:openaccessSDNB:540institution:unirostock.mnfstate:published