Hochschulschrift
Advances in alkyne metathesis: catalysts with multivalent siloxy ligands & formal total synthesis of (+)-aspicilin & stabilization of α-helical peptide structures
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
-
Englisch
- Notes
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Dortmund, Technische Universität, Dissertation, 2016
- Classification
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Chemie
- Event
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Veröffentlichung
- (where)
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Dortmund
- (who)
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Universitätsbibliothek Dortmund
- (when)
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2016
- Creator
- Contributor
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Fürstner, Alois
Hiersemann, Martin
- Handle
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2003/35119
- URN
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urn:nbn:de:101:1-201608293204
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:45 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
- Schaubach, Sebastian
- Fürstner, Alois
- Hiersemann, Martin
- Universitätsbibliothek Dortmund
Time of origin
- 2016
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A Sphingolipid Fatty Acid Constituent Made by Alkyne trans ‐Hydrogenation: Total Synthesis of Symbioramide
How to Break the Law: trans ‐Hydroboration and gem ‐Hydroboration of Alkynes
Light‐Driven gem Hydrogenation: An Orthogonal Entry into “Second‐Generation” Ruthenium Carbene Catalysts for Olefin Metathesis
183 W NMR Spectroscopy Guides the Search for Tungsten Alkylidyne Catalysts for Alkyne Metathesis
183 W NMR Spectroscopy Guides the Search for Tungsten Alkylidyne Catalysts for Alkyne Metathesis
An Alkyne‐Metathesis‐Based Approach to the Synthesis of the Anti‐Malarial Macrodiolide Samroiyotmycin A
An Alkyne‐Metathesis‐Based Approach to the Synthesis of the Anti‐Malarial Macrodiolide Samroiyotmycin A
Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes
Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes
Canopy Catalysts for Alkyne Metathesis: Investigations into a Bimolecular Decomposition Pathway and the Stability of the Podand Cap
Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts
Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts
A Sphingolipid Fatty Acid Constituent Made by Alkyne trans ‐Hydrogenation: Total Synthesis of Symbioramide
How to Break the Law: trans ‐Hydroboration and gem ‐Hydroboration of Alkynes
Light‐Driven gem Hydrogenation: An Orthogonal Entry into “Second‐Generation” Ruthenium Carbene Catalysts for Olefin Metathesis
183 W NMR Spectroscopy Guides the Search for Tungsten Alkylidyne Catalysts for Alkyne Metathesis
183 W NMR Spectroscopy Guides the Search for Tungsten Alkylidyne Catalysts for Alkyne Metathesis
An Alkyne‐Metathesis‐Based Approach to the Synthesis of the Anti‐Malarial Macrodiolide Samroiyotmycin A
An Alkyne‐Metathesis‐Based Approach to the Synthesis of the Anti‐Malarial Macrodiolide Samroiyotmycin A
Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes
Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes
Canopy Catalysts for Alkyne Metathesis: Investigations into a Bimolecular Decomposition Pathway and the Stability of the Podand Cap
Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts
Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts
A Sphingolipid Fatty Acid Constituent Made by Alkyne trans ‐Hydrogenation: Total Synthesis of Symbioramide
How to Break the Law: trans ‐Hydroboration and gem ‐Hydroboration of Alkynes
Light‐Driven gem Hydrogenation: An Orthogonal Entry into “Second‐Generation” Ruthenium Carbene Catalysts for Olefin Metathesis
183 W NMR Spectroscopy Guides the Search for Tungsten Alkylidyne Catalysts for Alkyne Metathesis
183 W NMR Spectroscopy Guides the Search for Tungsten Alkylidyne Catalysts for Alkyne Metathesis
An Alkyne‐Metathesis‐Based Approach to the Synthesis of the Anti‐Malarial Macrodiolide Samroiyotmycin A
An Alkyne‐Metathesis‐Based Approach to the Synthesis of the Anti‐Malarial Macrodiolide Samroiyotmycin A
Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes
Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes