mycoreobjectrosdok_disshab_0000001298rosdok_disshab_0000001298rosdokdisshabrosdok_derivate_00000238132023-08-08T10:05:37.411Z2015-02-10T14:07:20.057ZadministratoreditorDpublished1rosdok_derivate_0000023813truetruederivate_types:fulltextVolltextfulltextwf_edit_epub wf_register_epubstate:publishedstate:publishedveröffentlichtpublishedrosdok/id00001477817979123MODS updated during RosDok migration in June 2021DissertationHochschulschrift1064970052SatenikMkrtchyan1986-VerfasserInautExploration of new sustainable synthetic methods for the synthesis of fused pyridines and 4-quinolones based on the domino reaction of chromones and other masked dielectrophiles with nucleophilesen132314614Prof. Dr.PeterLangerUniversity of Rostock, Faculty of ChemistryAkademischeR BetreuerIndgsProf. Dr.BerndSchmidtUniversity of Potsdam, Faculty of ChemistryAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00001477http://purl.uni-rostock.de/rosdok/id00001477urn:nbn:de:gbv:28-diss2015-0027-2540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2015monographic20142015Universitätsbibliothek RostockRostock20152015The present work aimed to study the big potential of chromone derivatives and 1-(2-fluorophenyl)prop-2-yn-1-ones for the synthesis of purine-like fused pyridines and 4-quinolone derivatives. In this regard, a wide range of substituents and substitution patterns are tolerated in the reaction. In addition a new and easy way for synthesis of 4-quinolone derivatives and other fused systems via domino cycloaddition reactions of ortho-fluoro substituted benzoylchromones, 1-(2-fluorophenyl)prop-2-yn-1-ones and aliphatic or aromatic amines were developed.[3+3] domino cleavagepurine-likeortho-fluorine-substituted benzoylchromonesUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00001477doctype: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/Exploration of new sustainable synthetic methods for the synthesis of fused pyridines and 4-quinolones based on the domino reaction of chromones and other masked dielectrophiles with nucleophilesExploration of new sustainable synthetic methods for the synthesis of fused pyridines and 4-quinolones based on the domino reaction of chromones and other masked dielectrophiles with nucleophilesgnd:1064970052gnd:132314614gnd:2147083-2gnd:1064970052gnd:132314614gnd:2147083-2rosdok_disshab_0000001298-d954447e39gnd:1064970052Satenik MkrtchyanSatenik Mkrtchyanrosdok_disshab_0000001298-d954447e60gnd:132314614Prof. Dr. Peter LangerProf. Dr. Peter Langerrosdok_disshab_0000001298-d954447e75Prof. Dr. Bernd SchmidtProf. Dr. Bernd Schmidtrosdok_disshab_0000001298-d954447e88gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätSatenik MkrtchyanProf. Dr. Peter LangerProf. Dr. Bernd SchmidtUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätSatenik MkrtchyanProf. Dr. Peter LangerProf. Dr. Bernd SchmidtUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätSatenik MkrtchyanRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00001477http://purl.uni-rostock.de/rosdok/id00001477urn:nbn:de:gbv:28-diss2015-0027-2[3+3] domino cleavagepurine-likeortho-fluorine-substituted benzoylchromonesThe present work aimed to study the big potential of chromone derivatives and 1-(2-fluorophenyl)prop-2-yn-1-ones for the synthesis of purine-like fused pyridines and 4-quinolone derivatives. In this regard, a wide range of substituents and substitution patterns are tolerated in the reaction. In addition a new and easy way for synthesis of 4-quinolone derivatives and other fused systems via domino cycloaddition reactions of ortho-fluoro substituted benzoylchromones, 1-(2-fluorophenyl)prop-2-yn-1-ones and aliphatic or aromatic amines were developed.20152015epub.dissertation1 Dissertation_Mkrtchyan_2015.pdf 6821443 aec90bc18e485e211793e4d74608f13b rosdok/id00001477817979123MODS updated during RosDok migration in June 2021DissertationHochschulschrift1064970052SatenikMkrtchyan1986-VerfasserInautExploration of new sustainable synthetic methods for the synthesis of fused pyridines and 4-quinolones based on the domino reaction of chromones and other masked dielectrophiles with nucleophilesen132314614Prof. Dr.PeterLangerUniversity of Rostock, Faculty of ChemistryAkademischeR BetreuerIndgsProf. Dr.BerndSchmidtUniversity of Potsdam, Faculty of ChemistryAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00001477http://purl.uni-rostock.de/rosdok/id00001477urn:nbn:de:gbv:28-diss2015-0027-2540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2015monographic20142015Universitätsbibliothek RostockRostock20152015The present work aimed to study the big potential of chromone derivatives and 1-(2-fluorophenyl)prop-2-yn-1-ones for the synthesis of purine-like fused pyridines and 4-quinolone derivatives. In this regard, a wide range of substituents and substitution patterns are tolerated in the reaction. In addition a new and easy way for synthesis of 4-quinolone derivatives and other fused systems via domino cycloaddition reactions of ortho-fluoro substituted benzoylchromones, 1-(2-fluorophenyl)prop-2-yn-1-ones and aliphatic or aromatic amines were developed.[3+3] domino cleavagepurine-likeortho-fluorine-substituted benzoylchromonesUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00001477 2015-02-10T14:07:20.057Z 2023-08-08T10:05:37.411Z 2023-08-18T10:05:37.416Z editorD {"identifier":"rosdok/id00001477","type":"local_id","additional":"","service":"MCRLocalID","created":"2018-06-30T13:14:00.852Z"} {"identifier":"http://purl.uni-rostock.de/rosdok/id00001477","type":"purl","additional":"","service":"RosDokPURL","created":"2018-06-30T13:14:01.052Z","registered":"2018-06-30T13:14:01.052Z"} {"identifier":"10.18453/rosdok_id00001477","type":"doi","additional":"","service":"RosDokDOI","created":"2018-06-30T13:14:02.435Z","registered":"2018-06-30T13:14:02.435Z"} {"identifier":"urn:nbn:de:gbv:28-diss2015-0027-2","type":"dnbUrn","additional":"","service":"RosDokURN","created":"2018-06-30T13:14:00.858Z","registered":"2015-02-13T03:11:03.273Z"} administratorfulltextfile/rosdok_disshab_0000001298/rosdok_derivate_0000023813/Dissertation_Mkrtchyan_2015.pdfExploration of new sustainable synthetic methods for the synthesis of fused pyridines and 4-quinolones based on the domino reaction of chromones and other masked dielectrophiles with nucleophilesExploration of new sustainable synthetic methods for the synthesis of fused pyridines and 4-quinolones based on the domino reaction of chromones and other masked dielectrophiles with nucleophilesgnd:1064970052gnd:132314614gnd:2147083-2gnd:1064970052gnd:132314614gnd:2147083-2rosdok_disshab_0000001298-d954447e39gnd:1064970052Satenik MkrtchyanSatenik Mkrtchyanrosdok_disshab_0000001298-d954447e60gnd:132314614Prof. Dr. Peter LangerProf. Dr. Peter Langerrosdok_disshab_0000001298-d954447e75Prof. Dr. Bernd SchmidtProf. Dr. Bernd Schmidtrosdok_disshab_0000001298-d954447e88gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätSatenik MkrtchyanProf. Dr. Peter LangerProf. Dr. Bernd SchmidtUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätSatenik MkrtchyanProf. Dr. Peter LangerProf. Dr. Bernd SchmidtUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätSatenik MkrtchyanRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00001477http://purl.uni-rostock.de/rosdok/id00001477urn:nbn:de:gbv:28-diss2015-0027-2[3+3] domino cleavagepurine-likeortho-fluorine-substituted benzoylchromonesThe present work aimed to study the big potential of chromone derivatives and 1-(2-fluorophenyl)prop-2-yn-1-ones for the synthesis of purine-like fused pyridines and 4-quinolone derivatives. In this regard, a wide range of substituents and substitution patterns are tolerated in the reaction. In addition a new and easy way for synthesis of 4-quinolone derivatives and other fused systems via domino cycloaddition reactions of ortho-fluoro substituted benzoylchromones, 1-(2-fluorophenyl)prop-2-yn-1-ones and aliphatic or aromatic amines were developed.20152015[xslt]Saxonrosdok/id00001477https://purl.uni-rostock.de/rosdok/id0000147781797912310.18453/rosdok_id00001477urn:nbn:de:gbv:28-diss2015-0027-2Satenik MkrtchyanMkrtchyan SatenikExploration of new sustainable synthetic methods for the synthesis of fused pyridines and 4-quinolones based on the domino reaction of chromones and other masked dielectrophiles with nucleophilesDissertationdoctoral thesisUniversität Rostock, 2015The present work aimed to study the big potential of chromone derivatives and 1-(2-fluorophenyl)prop-2-yn-1-ones for the synthesis of purine-like fused pyridines and 4-quinolone derivatives. In this regard, a wide range of substituents and substitution patterns are tolerated in the reaction. In…Satenik MkrtchyanExploration of new sustainable synthetic methods for the synthesis of fused pyridines and 4-quinolones based on the domino reaction of chromones and other masked dielectrophiles with nucleophilesUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id000014771064970052SatenikMkrtchyan1986-VerfasserInaut132314614Prof. Dr.PeterLangerUniversity of Rostock, Faculty of ChemistryAkademischeR BetreuerIndgsProf. Dr.BerndSchmidtUniversity of Potsdam, Faculty of ChemistryAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg[doi]10.18453/rosdok_id00001477[purl]http://purl.uni-rostock.de/rosdok/id00001477[urn]urn:nbn:de:gbv:28-diss2015-0027-2open_access20152015epoch:21th_centuryrfc5646:endoctype:epub.dissertationaccesscondition:openaccessSDNB:540institution:unirostock.mnfstate:published