mycoreobjectrosdok_disshab_0000001074rosdok_disshab_0000001074rosdokdisshabrosdok_derivate_00000052022023-08-08T10:04:30.436Z2014-01-10T11:27:47.415Zadministratorpublished1rosdok_derivate_0000005202truetruederivate_types:fulltextVolltextfulltextwf_edit_epub wf_register_epubstate:publishedstate:publishedveröffentlichtpublishedrosdok/id00001253776425390MODS updated during RosDok migration in June 2021DissertationHochschulschrift1046201883Jaya Shanmuga PrakashJegannathan1982-VerfasserInautImproved synthesis of 2,3-diacetamidouronates which are present in bacterial envelopeen1011717204Prof. Dr.ChristianVogelUniversity of Rostock, Institute of Organic ChemistryAkademischeR BetreuerIndgs122688511Prof. Dr.TillOpatzUniversity of Mainz, Institute of Organic ChemistryAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg10.18453/rosdok_id00001253http://purl.uni-rostock.de/rosdok/id00001253urn:nbn:de:gbv:28-diss2014-0005-4540 ChemieMathematisch-Naturwissenschaftliche Fakultätfrei zugänglich (Open Access)Lizenz Metadaten: CC0Nutzungsrechte erteiltalle Rechte vorbehaltenUniversität RostockRostock2014monographic20132014Universitätsbibliothek RostockRostock20142014Diacetamidodideoxyuronic acids are components of lipopolysaccarides present in bacterial cell wall. There are very few publications reporting the preparation of this class of sugars. Hence, we present the synthesis of gluco-, galacto- and manno- configured sugars of 2,3-diacetamido-2,3-dideoxy-D-uronates. These monosaccharaides can be employed as glycosyl donors and acceptors in glycosylation reactions to produce larger glycosylates which can serve as components of antibiotics. Currently, the target molecules were synthesized in high yields with good reproducibility and scalability.carbohydrate chemistrytotal synthesisbio-organic chemistryUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id00001253doctype: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/Improved synthesis of 2,3-diacetamidouronates which are present in bacterial envelopeImproved synthesis of 2,3-diacetamidouronates which are present in bacterial envelopegnd:1046201883gnd:1011717204gnd:122688511gnd:2147083-2gnd:1046201883gnd:1011717204gnd:122688511gnd:2147083-2rosdok_disshab_0000001074-d705926e39gnd:1046201883Jaya Shanmuga Prakash JegannathanJaya Shanmuga Prakash Jegannathanrosdok_disshab_0000001074-d705926e60gnd:1011717204Prof. Dr. Christian VogelProf. Dr. Christian Vogelrosdok_disshab_0000001074-d705926e75gnd:122688511Prof. Dr. Till OpatzProf. Dr. Till Opatzrosdok_disshab_0000001074-d705926e90gnd:2147083-2Universität Rostock Mathematisch-Naturwissenschaftliche FakultätUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätJaya Shanmuga Prakash JegannathanProf. Dr. Christian VogelProf. Dr. Till OpatzUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätJaya Shanmuga Prakash JegannathanProf. Dr. Christian VogelProf. Dr. Till OpatzUniversität Rostock Mathematisch-Naturwissenschaftliche FakultätJaya Shanmuga Prakash JegannathanRostockUniversität Rostockepub.dissertation10.18453/rosdok_id00001253http://purl.uni-rostock.de/rosdok/id00001253urn:nbn:de:gbv:28-diss2014-0005-4carbohydrate chemistrytotal synthesisbio-organic chemistryDiacetamidodideoxyuronic acids are components of lipopolysaccarides present in bacterial cell wall. There are very few publications reporting the preparation of this class of sugars. Hence, we present the synthesis of gluco-, galacto- and manno- configured sugars of 2,3-diacetamido-2,3-dideoxy-D-uronates. These monosaccharaides can be employed as glycosyl donors and acceptors in glycosylation reactions to produce larger glycosylates which can serve as components of antibiotics. 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There are very few publications reporting the preparation of this class of sugars. Hence, we present the synthesis of gluco-, galacto- and manno- configured sugars of 2,3-diacetamido-2,3-dideoxy-D-uronates. These monosaccharaides can be employed as glycosyl donors and acceptors in glycosylation reactions to produce larger glycosylates which can serve as components of antibiotics. 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There are very few publications reporting the preparation of this class of sugars. Hence, we present the synthesis of gluco-, galacto- and manno- configured sugars of 2,3-diacetamido-2,3-dideoxy-D-uronates. These monosaccharaides can be employed as glycosyl donors and acceptors in glycosylation reactions to produce larger glycosylates which can serve as components of antibiotics. Currently, the target molecules were synthesized in high yields with good reproducibility and scalability.20142014[xslt]Saxonrosdok/id00001253https://purl.uni-rostock.de/rosdok/id0000125377642539010.18453/rosdok_id00001253urn:nbn:de:gbv:28-diss2014-0005-4Jaya Shanmuga Prakash JegannathanJegannathan Jaya Shanmuga PrakashImproved synthesis of 2,3-diacetamidouronates which are present in bacterial envelopeDissertationdoctoral thesisUniversität Rostock, 2014Diacetamidodideoxyuronic acids are components of lipopolysaccarides present in bacterial cell wall. There are very few publications reporting the preparation of this class of sugars. Hence, we present the synthesis of gluco-, galacto- and manno- configured sugars of…Jaya Shanmuga Prakash JegannathanImproved synthesis of 2,3-diacetamidouronates which are present in bacterial envelopeUniversitätsbibliothek Rostockhttp://purl.uni-rostock.de/rosdok/id000012531046201883Jaya Shanmuga PrakashJegannathan1982-VerfasserInaut1011717204Prof. Dr.ChristianVogelUniversity of Rostock, Institute of Organic ChemistryAkademischeR BetreuerIndgs122688511Prof. Dr.TillOpatzUniversity of Mainz, Institute of Organic ChemistryAkademischeR BetreuerIndgs2147083-2Universität RostockMathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgg[doi]10.18453/rosdok_id00001253[purl]http://purl.uni-rostock.de/rosdok/id00001253[urn]urn:nbn:de:gbv:28-diss2014-0005-4open_access20142014epoch:21th_centuryrfc5646:endoctype:epub.dissertationaccesscondition:openaccessSDNB:540institution:unirostock.mnfstate:published