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Enantioselektive Synthese mono- und tricyclischer gamma-Butyrolacton-Naturstoffe

Nosse, Bernd (2005) Enantioselektive Synthese mono- und tricyclischer gamma-Butyrolacton-Naturstoffe. PhD, Universität Regensburg.

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Date of publication of this fulltext: 14 Nov 2005 06:51

Abstract (German)

Etwa 10 % aller bekannten Naturstoffe beinhalten eine gamma-Butyrolactoneinheit entweder als charakteristisches Strukturelement oder als zentrale Einheit. Die im Rahmen dieser Dissertation durchgeführten Untersuchungen hatten die Entwicklung von Methoden zur enantioselektiven Synthese von mono- und tricyclischen (5.6.5, 5.6.6 oder 5.7.5) Ringsystemen zum Ziel. Diese beinhalten ein ...


Translation of the abstract (English)

About 10% of all known natural products have been found to contain gamma-butyrolactones as part of simple or more complex systems. The studies in this thesis are directed towards the development of convenient methodologies for the synthesis of monocyclic and tricyclic (5.6.5, 5.6.6 or 5.7.5) ring systems containing trans-2,3-disubstituted lactones, such as can be found in paraconic acids ...


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Item type:Thesis of the University of Regensburg (PhD)
Date:13 November 2005
Referee:Oliver (Prof. Dr.) Reiser
Date of exam:11 November 2004
Institutions:Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Oliver Reiser
Keywords:Naturstoff , Butyrolactone , Ringschlussmetathese , Paraconsäure , Guaianolide , Sakurai Allylierung , Carbonyl-En , Eudesmanolide , Arglabin , Ixerin Y , Protopraesorediosinsäure , natural product , gamma-butyrolactone , ring closing metathesis , arglabin , farnesyl transferase inhibitor
Dewey Decimal Classification:500 Science > 540 Chemistry & allied sciences
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Yes
Item ID:10277
Owner only: item control page


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