mycoreobjectrosdok_disshab_0000002056rosdok_disshab_0000002056rosdokdisshabrosdok_derivate_00000659642023-08-08T10:09:49.398Z2019-02-13T07:11:52.510ZadministratoreditorDpublished1rosdok_derivate_0000065964truetruederivate_types:fulltextVolltextfulltextwf_edit_epub wf_register_epubstate:publishedstate:publishedveröffentlichtpublishedrosdok/id000024031048999467Oau2019-02-132023-08-05T19:11:58ZrdaConverted from PICA to MODS using Pica2Mods XSLT Transformer 2.7 [SCM: "0c0e7a3c226a4a0cbcbec39b493c3c5257339ab8" "v2.7" "2023-08-04T00:00:00+0200"] with mode 'DEFAULT'.DissertationHochschulschriftBio-based building blocks from 5-hydroxymethylfurfural via 1-hydroxyhexane-2,5-dione as intermediateThis dissertation reports on the synthesis and applications of the biomass-derived 1-hydroxyhexane-2,5-dione (HHD). A new catalytic process was developed for the hydrogenation/hydrolytic ring opening of 5-hydroxymethylfurfural (5-HMF) resulting in the formation of HHD in good yields. Furthermore, HHD was converted to useful follow-up products including pyrroles and cyclopentanone derivatives. Additionally, readily accessible rhenium(VII) oxide was used for the catalytic deoxydehydration of renewable triols under solvent-free and aerobic conditions resulting in formation of the hydroxy-alkenes.BartoszWoźniak1991 -VerfasserInaut117790103XJohannesVriesdeAkademischeR BetreuerIndgsKatalinBarta1980 -AkademischeR BetreuerIndgs13611478438329-6Universität Rostock1419 -Grad-verleihende Institutiondgg2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgghttp://purl.uni-rostock.de/rosdok/id00002403urn:nbn:de:gbv:28-rosdok_id00002403-710.18453/rosdok_id00002403540 ChemieMathematisch-Naturwissenschaftliche Fakultätalle Rechte vorbehaltenNutzungsrechte erteiltLizenz Metadaten: CC0frei zugänglich (Open Access)en2018Universität RostockRostockmonographic201920182019Universitätsbibliothek RostockRostock2019Universitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00002403Die Dissertation enthält Zeitschriftenartikel.vorgelegt von Bartosz WozniakHydrierungKatalysatordoctype: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 thesisSDNB: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/2147083-2licenseinfo: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/licenseinfo:depositlicenseinfo:depositVeröffentlichungsgenehmigungpermission to storelicenseinfo:deposit.rightsgrantedlicenseinfo:deposit.rightsgrantedNutzungsrechte erteiltrights grantedlicenseinfo: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/accesscondition: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_abf2rfc5646:enrfc5646:enEnglischEnglishengengBio-based building blocks from 5-hydroxymethylfurfural via 1-hydroxyhexane-2,5-dione as intermediateBio-based building blocks from 5-hydroxymethylfurfural via 1-hydroxyhexane-2,5-dione as intermediategnd:117790103Xgnd:136114784gnd:38329-6gnd:2147083-2gnd:117790103Xgnd:136114784gnd:38329-6gnd:2147083-2rosdok_disshab_0000002056-d3917284e52gnd:117790103XBartosz WoźniakBartosz Woźniakrosdok_disshab_0000002056-d3917284e66Johannes Vries deJohannes Vries derosdok_disshab_0000002056-d3917284e78gnd:136114784Katalin BartaKatalin Bartarosdok_disshab_0000002056-d3917284e92gnd:38329-6Universität RostockUniversität Rostockrosdok_disshab_0000002056-d3917284e104gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätBartosz WoźniakJohannes Vries deKatalin BartaUniversität RostockUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätBartosz WoźniakJohannes Vries deKatalin BartaUniversität RostockUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätBartosz WoźniakRostockUniversität Rostockepub.dissertationhttp://purl.uni-rostock.de/rosdok/id00002403urn:nbn:de:gbv:28-rosdok_id00002403-710.18453/rosdok_id00002403HydrierungKatalysatorThis dissertation reports on the synthesis and applications of the biomass-derived 1-hydroxyhexane-2,5-dione (HHD). A new catalytic process was developed for the hydrogenation/hydrolytic ring opening of 5-hydroxymethylfurfural (5-HMF) resulting in the formation of HHD in good yields. Furthermore, HHD was converted to useful follow-up products including pyrroles and cyclopentanone derivatives. Additionally, readily accessible rhenium(VII) oxide was used for the catalytic deoxydehydration of renewable triols under solvent-free and aerobic conditions resulting in formation of the hydroxy-alkenes.20182018Die Dissertation enthält Zeitschriftenartikel.vorgelegt von Bartosz Wozniakepub.dissertation1 Wozniak_Dissertation_2019.pdf 6777847 6f247a3117abcb2bcc4335ea854c2b4c rosdok/id000024031048999467Oau2019-02-132023-08-05T19:11:58ZrdaConverted from PICA to MODS using Pica2Mods XSLT Transformer 2.7 [SCM: "0c0e7a3c226a4a0cbcbec39b493c3c5257339ab8" "v2.7" "2023-08-04T00:00:00+0200"] with mode 'DEFAULT'.DissertationHochschulschriftBio-based building blocks from 5-hydroxymethylfurfural via 1-hydroxyhexane-2,5-dione as intermediateThis dissertation reports on the synthesis and applications of the biomass-derived 1-hydroxyhexane-2,5-dione (HHD). A new catalytic process was developed for the hydrogenation/hydrolytic ring opening of 5-hydroxymethylfurfural (5-HMF) resulting in the formation of HHD in good yields. Furthermore, HHD was converted to useful follow-up products including pyrroles and cyclopentanone derivatives. Additionally, readily accessible rhenium(VII) oxide was used for the catalytic deoxydehydration of renewable triols under solvent-free and aerobic conditions resulting in formation of the hydroxy-alkenes.BartoszWoźniak1991 -VerfasserInaut117790103XJohannesVriesdeAkademischeR BetreuerIndgsKatalinBarta1980 -AkademischeR BetreuerIndgs13611478438329-6Universität Rostock1419 -Grad-verleihende Institutiondgg2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgghttp://purl.uni-rostock.de/rosdok/id00002403urn:nbn:de:gbv:28-rosdok_id00002403-710.18453/rosdok_id00002403540 ChemieMathematisch-Naturwissenschaftliche Fakultätalle Rechte vorbehaltenNutzungsrechte erteiltLizenz Metadaten: CC0frei zugänglich (Open Access)en2018Universität RostockRostockmonographic201920182019Universitätsbibliothek RostockRostock2019Universitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00002403Die Dissertation enthält Zeitschriftenartikel.vorgelegt von Bartosz WozniakHydrierungKatalysator 2019-02-13T07:11:52.510Z 2023-08-08T10:09:49.398Z 2023-08-18T10:09:49.403Z {"identifier":"rosdok/id00002403","type":"local_id","additional":"","service":"MCRLocalID","created":"2019-02-13T07:11:52.582Z"} editorD {"identifier":"http://purl.uni-rostock.de/rosdok/id00002403","type":"purl","additional":"","service":"RosDokPURL","created":"2019-02-13T07:23:56.590Z","registered":"2019-02-13T07:23:56.590Z"} {"identifier":"10.18453/rosdok_id00002403","type":"doi","additional":"","service":"RosDokDOI","created":"2019-02-13T07:23:58.021Z","registered":"2019-02-13T07:23:58.021Z"} {"identifier":"urn:nbn:de:gbv:28-rosdok_id00002403-7","type":"dnbUrn","additional":"","service":"RosDokURN","created":"2019-02-13T07:11:52.654Z","registered":"2019-02-14T03:22:10.283Z"} administratorfulltextfile/rosdok_disshab_0000002056/rosdok_derivate_0000065964/Wozniak_Dissertation_2019.pdfBio-based building blocks from 5-hydroxymethylfurfural via 1-hydroxyhexane-2,5-dione as intermediateBio-based building blocks from 5-hydroxymethylfurfural via 1-hydroxyhexane-2,5-dione as intermediategnd:117790103Xgnd:136114784gnd:38329-6gnd:2147083-2gnd:117790103Xgnd:136114784gnd:38329-6gnd:2147083-2rosdok_disshab_0000002056-d3917284e52gnd:117790103XBartosz WoźniakBartosz Woźniakrosdok_disshab_0000002056-d3917284e66Johannes Vries deJohannes Vries derosdok_disshab_0000002056-d3917284e78gnd:136114784Katalin BartaKatalin Bartarosdok_disshab_0000002056-d3917284e92gnd:38329-6Universität RostockUniversität Rostockrosdok_disshab_0000002056-d3917284e104gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätBartosz WoźniakJohannes Vries deKatalin BartaUniversität RostockUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätBartosz WoźniakJohannes Vries deKatalin BartaUniversität RostockUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätBartosz WoźniakRostockUniversität Rostockepub.dissertationhttp://purl.uni-rostock.de/rosdok/id00002403urn:nbn:de:gbv:28-rosdok_id00002403-710.18453/rosdok_id00002403HydrierungKatalysatorThis dissertation reports on the synthesis and applications of the biomass-derived 1-hydroxyhexane-2,5-dione (HHD). A new catalytic process was developed for the hydrogenation/hydrolytic ring opening of 5-hydroxymethylfurfural (5-HMF) resulting in the formation of HHD in good yields. Furthermore, HHD was converted to useful follow-up products including pyrroles and cyclopentanone derivatives. Additionally, readily accessible rhenium(VII) oxide was used for the catalytic deoxydehydration of renewable triols under solvent-free and aerobic conditions resulting in formation of the hydroxy-alkenes.20182018Die Dissertation enthält Zeitschriftenartikel.vorgelegt von Bartosz Wozniak[xslt]Saxonrosdok/id00002403https://purl.uni-rostock.de/rosdok/id00002403104899946710.18453/rosdok_id00002403urn:nbn:de:gbv:28-rosdok_id00002403-7Bartosz WoźniakWoźniak BartoszBio-based building blocks from 5-hydroxymethylfurfural via 1-hydroxyhexane-2,5-dione as intermediateDissertationdoctoral thesisUniversität Rostock, 2018This dissertation reports on the synthesis and applications of the biomass-derived 1-hydroxyhexane-2,5-dione (HHD). A new catalytic process was developed for the hydrogenation/hydrolytic ring opening of 5-hydroxymethylfurfural (5-HMF) resulting in the formation of HHD in good yields. Furthermore,…Bartosz WoźniakBio-based building blocks from 5-hydroxymethylfurfural via 1-hydroxyhexane-2,5-dione as intermediateUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00002403BartoszWoźniak1991 -VerfasserInaut117790103XJohannesVriesdeAkademischeR BetreuerIndgsKatalinBarta1980 -AkademischeR BetreuerIndgs13611478438329-6Universität Rostock1419 -Grad-verleihende Institutiondgg2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg[purl]http://purl.uni-rostock.de/rosdok/id00002403[urn]urn:nbn:de:gbv:28-rosdok_id00002403-7[doi]10.18453/rosdok_id00002403open_access20182018epoch:21th_centuryrfc5646:endoctype:epub.dissertationaccesscondition:openaccessSDNB:540institution:unirostock.mnfstate:published