Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts ; volume:131 ; number:44 ; year:2019 ; pages:15837-15843 ; extent:7
Angewandte Chemie ; 131, Heft 44 (2019), 15837-15843 (gesamt 7)
- Creator
- DOI
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10.1002/ange.201908571
- URN
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urn:nbn:de:101:1-2022080107213322913640
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:34 AM CEST
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Hillenbrand, Julius
- Leutzsch, Markus
- Fürstner, Alois
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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
Advances in alkyne metathesis: catalysts with multivalent siloxy ligands & formal total synthesis of (+)-aspicilin & stabilization of α-helical peptide structures
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
Advances in alkyne metathesis: catalysts with multivalent siloxy ligands & formal total synthesis of (+)-aspicilin & stabilization of α-helical peptide structures
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