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dc.contributor.advisor Tietze, Lutz Prof. Dr. Dr. h.c.
dc.contributor.author Heidemann, Sven
dc.date.accessioned 2016-10-10T08:49:28Z
dc.date.available 2016-10-10T08:49:28Z
dc.date.issued 2016-10-10
dc.identifier.uri http://hdl.handle.net/11858/00-1735-0000-002B-7C16-4
dc.language.iso deu de
dc.publisher Niedersächsische Staats- und Universitätsbibliothek Göttingen de
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc 540 de
dc.title Untersuchungen zur enantioselektiven Totalsynthese von Parnafungin C de
dc.type doctoralThesis de
dc.title.translated Studies towards the Enantioselective Total Synthesis of Parnafungin C de
dc.contributor.referee Tietze, Lutz Prof. Dr. Dr. H.c.
dc.date.examination 2016-08-04
dc.description.abstracteng Within this thesis, two fragments of the natural product Parnafungin C, a highly functionalized chiral chromane with the correct absolute and relative configuration of all stereogenic centers as well as a biaryl system comprising all required substituents for the formation of the unique isoxazolidinone-moiety, were synthesized. Key steps are an enantioselective Wacker oxidation or a Domino-Wacker/carbonylation/methoxylation reaction, a Sharpless asymmetric dihydroxylation reaction and a Suzuki-Miyaura cross coupling reaction. de
dc.contributor.coReferee Diederichsen, Ulf Prof. Dr.
dc.subject.eng Parnafungin C de
dc.subject.eng Enantioselective Total Synthesis de
dc.subject.eng Wacker oxidation de
dc.subject.eng Domino reaction de
dc.subject.eng Suzuki-Miyaura cross coupling de
dc.subject.eng Sharpless dihydroxylation de
dc.identifier.urn urn:nbn:de:gbv:7-11858/00-1735-0000-002B-7C16-4-9
dc.affiliation.institute Fakultät für Chemie de
dc.subject.gokfull Chemie  (PPN62138352X) de
dc.identifier.ppn 869904310

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