Item type:Doctoral Thesis, Open Access

Die Totalsynthese von Cladoniamid G und Cladoniamid F

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Date

2014-06-05

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Philipps-Universität Marburg
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Abstract

This dissertation describes the total synthesis of two natural products cladoniamide G and cladoniamide F which belong to the group of indenotryptolines that is closely related to the natural product class of indolocarbazoles. Key steps of the synthesis were the addition of an indole to a mesoxalic ester amide, a Suzuki cross-coupling of two indoles and an intramolecular lactam formation. Additionally, a method for the enantioselective addtion of indoles to mesoxalic ester amides was developed.

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Dates
Created: 2014Issued: 2014-06-05Updated: 2014-06-05
DOI
https://doi.org/10.17192/z2014.0251
Faculty
Fachbereich Chemie
Publisher
Philipps-Universität Marburg
Language
ger
Data types
DoctoralThesis
Keywords
IndenotryptolinesIndenotryptolinNatural ProductsIndolocarbazolTotal Synthesis
DFG-subjects
IndolTotalsyntheseNaturstoff
DDC-Numbers
500
License
https://rightsstatements.org/vocab/InC-NC/1.0/
URI
https://open.uni-marburg.de/handle/10.17192/z2014.0251
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Schütte, Julia (1042030200): Die Totalsynthese von Cladoniamid G und Cladoniamid F. : Philipps-Universität Marburg 2014-06-05. DOI: https://doi.org/10.17192/z2014.0251.

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