Show simple item record

Domino Reactions for the Syntheses of Chiral Chromanes ‒ Enantioselective Total Syntheses of (‒)-Diversonol, (‒)-Blennolide C, (‒)-Gonytolide C and Formal Synthesis of Siccanin

dc.contributor.advisorTietze, Lutz Prof. Dr. Dr. h.c.
dc.contributor.authorJackenkroll, Stefan
dc.date.accessioned2015-06-15T09:01:28Z
dc.date.available2015-06-15T09:01:28Z
dc.date.issued2015-06-15
dc.identifier.urihttp://hdl.handle.net/11858/00-1735-0000-0022-601F-0
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-5135
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-5135
dc.language.isoengde
dc.publisherNiedersächsische Staats- und Universitätsbibliothek Göttingende
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc540de
dc.titleDomino Reactions for the Syntheses of Chiral Chromanes ‒ Enantioselective Total Syntheses of (‒)-Diversonol, (‒)-Blennolide C, (‒)-Gonytolide C and Formal Synthesis of Siccaninde
dc.typedoctoralThesisde
dc.contributor.refereeTietze, Lutz Prof. Dr. Dr. h.c.
dc.date.examination2014-07-28
dc.description.abstractengThe general objective of this thesis is to demonstrate the synthetic utility of the domino concept in the complex setting of natural product synthesis. Key step is a palladium-catalyzed domino Wacker/carbonylation/methoxylation reaction that was successfully applied in the enantioselective total syntheses of (‒)-diversonol, (‒)-blennolide C and (‒)-gonytolide C as well as in the formal synthesis of siccanin.de
dc.contributor.coRefereeWerz, Daniel Prof. Dr.
dc.subject.engdomino reactionsde
dc.subject.engpalladiumde
dc.subject.engtotal synthesisde
dc.subject.engWacker oxidationde
dc.identifier.urnurn:nbn:de:gbv:7-11858/00-1735-0000-0022-601F-0-4
dc.affiliation.instituteFakultät für Chemiede
dc.subject.gokfullChemie  (PPN62138352X)de
dc.identifier.ppn82741594X


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record