Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes
- 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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Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes ; volume:59 ; number:42 ; year:2020 ; pages:18423-18429 ; extent:7
Angewandte Chemie / International edition. International edition ; 59, Heft 42 (2020), 18423-18429 (gesamt 7)
- Creator
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Biberger, Tobias
Zachmann, Raphael J.
Fürstner, Alois
- DOI
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10.1002/anie.202007030
- URN
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urn:nbn:de:101:1-2022062212555408571006
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:33 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Biberger, Tobias
- Zachmann, Raphael J.
- Fürstner, Alois
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Mechanistic Divergence in the Hydrogenative Synthesis of Furans and Butenolides: Ruthenium Carbenes Formed by gem ‐Hydrogenation or through Carbophilic Activation of Alkynes
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Total Synthesis of the Marine Diterpenoids Caucanolide E and F by Alkyne gem ‐Hydrogenation: Rigorous Reassignment of Two Almost Indistinguishable Diastereomers
SYNTHESIS Special Issue in Honor of Professor Sarah Reisman
Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes
Light‐Driven gem Hydrogenation: An Orthogonal Entry into “Second‐Generation” Ruthenium Carbene Catalysts for Olefin Metathesis
How to Break the Law: trans ‐Hydroboration and gem ‐Hydroboration of Alkynes
Mechanistic Divergence in the Hydrogenative Synthesis of Furans and Butenolides: Ruthenium Carbenes Formed by gem ‐Hydrogenation or through Carbophilic Activation of Alkynes
Light‐Driven Alkyne gem ‐Hydrogenation: An Intramolecular Approach to Hoveyda–Grubbs Catalysts
A Sphingolipid Fatty Acid Constituent Made by Alkyne trans ‐Hydrogenation: Total Synthesis of Symbioramide
Regioselective trans ‐Hydrostannation of Boron‐Capped Alkynes
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
Total Synthesis of the Marine Diterpenoids Caucanolide E and F by Alkyne gem ‐Hydrogenation: Rigorous Reassignment of Two Almost Indistinguishable Diastereomers
Total Synthesis of the Marine Diterpenoids Caucanolide E and F by Alkyne gem ‐Hydrogenation: Rigorous Reassignment of Two Almost Indistinguishable Diastereomers
SYNTHESIS Special Issue in Honor of Professor Sarah Reisman
Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes
Light‐Driven gem Hydrogenation: An Orthogonal Entry into “Second‐Generation” Ruthenium Carbene Catalysts for Olefin Metathesis
How to Break the Law: trans ‐Hydroboration and gem ‐Hydroboration of Alkynes
Mechanistic Divergence in the Hydrogenative Synthesis of Furans and Butenolides: Ruthenium Carbenes Formed by gem ‐Hydrogenation or through Carbophilic Activation of Alkynes
Light‐Driven Alkyne gem ‐Hydrogenation: An Intramolecular Approach to Hoveyda–Grubbs Catalysts
A Sphingolipid Fatty Acid Constituent Made by Alkyne trans ‐Hydrogenation: Total Synthesis of Symbioramide
Regioselective trans ‐Hydrostannation of Boron‐Capped Alkynes
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
Total Synthesis of the Marine Diterpenoids Caucanolide E and F by Alkyne gem ‐Hydrogenation: Rigorous Reassignment of Two Almost Indistinguishable Diastereomers
Total Synthesis of the Marine Diterpenoids Caucanolide E and F by Alkyne gem ‐Hydrogenation: Rigorous Reassignment of Two Almost Indistinguishable Diastereomers