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Stereoselektive Synthese von (7'R)-Hydroxyenterolacton, (7'R)-Parabenzlacton und (+)/(-)-Arteludovicinolid A

Kreuzer, Andreas (2016) Stereoselektive Synthese von (7'R)-Hydroxyenterolacton, (7'R)-Parabenzlacton und (+)/(-)-Arteludovicinolid A. PhD, Universität Regensburg.

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Date of publication of this fulltext: 02 Jun 2016 11:25

Abstract (German)

Ziel dieser Arbeit war es aus dem, aus nachwachsenden Rohstoffen erhältlichen, 2-Furancarbonsäuremethylester neue Synthesestrategien für die asymmetrischen Synthese von (7’R)-Hydroxyenterolacton, (7’R)-Parabenzlacton and Arteludovicinolid A zu entwickeln. Als chirale Ausgangsverbindung für alle drei Synthesen wurde ein Cyclopropanaldehyd eingesetzt, der in der Arbeitsgruppe Reiser bereits in ...

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Translation of the abstract (English)

The aims of this work were the development of synthetic strategies for the asymmetric synthesis of (7’R)-Hydroxyenterolactone, (7’R)-Parabenzlactone and Arteludovicinolide A from the renewable furoic ester 2-Methylfuroate. The chiral starting compond therfore, a cyclopropanaldehyde, was accessed via a two-step methodology consisting of an enantioselective cyclopropanation and a reductive ...

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Item type:Thesis of the University of Regensburg (PhD)
Date:1 June 2016
Referee:Prof. Dr. Oliver Reiser
Date of exam:27 April 2015
Institutions:Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Oliver Reiser
Keywords:Totalsynthese, Naturstoffsynthese, Arteludovicinolid A, Sesquiterpenlactone, Lignanolactone
Dewey Decimal Classification:500 Science > 540 Chemistry & allied sciences
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Yes
Item ID:31802
Owner only: item control page

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