Hydrogenative Cycloisomerization and Sigmatropic Rearrangement Reactions of Cationic Ruthenium Carbenes Formed by Catalytic Alkyne gem ‐Hydrogenation
- 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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Hydrogenative Cycloisomerization and Sigmatropic Rearrangement Reactions of Cationic Ruthenium Carbenes Formed by Catalytic Alkyne gem ‐Hydrogenation ; day:03 ; month:01 ; year:2022 ; extent:1
Angewandte Chemie / International edition. International edition ; (03.01.2022) (gesamt 1)
- Creator
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Biberger, Tobias
Hess, Stephan N.
Leutzsch, Markus
Fürstner, Alois
- DOI
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10.1002/anie.202113827
- URN
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urn:nbn:de:101:1-2022010414205865227393
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:35 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
- Hess, Stephan N.
- Leutzsch, Markus
- Fürstner, Alois
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Hydrogenative Cycloisomerization and Sigmatropic Rearrangement Reactions of Cationic Ruthenium Carbenes Formed by Catalytic Alkyne gem ‐Hydrogenation
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
Mechanistic Divergence in the Hydrogenative Synthesis of Furans and Butenolides: Ruthenium Carbenes Formed by gem ‐Hydrogenation or through Carbophilic Activation of 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
Light‐Driven Alkyne gem ‐Hydrogenation: An Intramolecular Approach to Hoveyda–Grubbs Catalysts
Light‐Driven gem Hydrogenation: An Orthogonal Entry into “Second‐Generation” Ruthenium Carbene Catalysts for Olefin Metathesis
An Efficient and Scalable “Second Generation” Total Synthesis of the Marine Polyketide Limaol Endowed with Antiparasitic Activity
Modular Synthesis of Furans with up to Four Different Substituents by a trans ‐Carboboration Strategy
Hydrogenative Cycloisomerization and Sigmatropic Rearrangement Reactions of Cationic Ruthenium Carbenes Formed by Catalytic Alkyne gem ‐Hydrogenation
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
Mechanistic Divergence in the Hydrogenative Synthesis of Furans and Butenolides: Ruthenium Carbenes Formed by gem ‐Hydrogenation or through Carbophilic Activation of 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
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