Untersuchungen zur enantioselektiven Totalsynthese von Parnafungin C

Heidemann, Sven

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.identifier.uri	http://dx.doi.org/10.53846/goediss-5881
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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Fakultät für Chemie (inkl. GAUSS) [702]

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