Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes ; volume:132 ; number:42 ; year:2020 ; pages:18581-18587 ; extent:7
Angewandte Chemie ; 132, Heft 42 (2020), 18581-18587 (gesamt 7)

Creator: Biberger, Tobias
Zachmann, Raphael J.
Fürstner, Alois

DOI: 10.1002/ange.202007030

URN: urn:nbn:de:101:1-2022052707055807527402

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:22 AM CEST

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Biberger, Tobias
Zachmann, Raphael J.
Fürstner, Alois

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Light‐Driven gem Hydrogenation: An Orthogonal Entry into “Second‐Generation” Ruthenium Carbene Catalysts for Olefin Metathesis

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Light‐Driven Alkyne gem ‐Hydrogenation: An Intramolecular Approach to Hoveyda–Grubbs Catalysts

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Regioselective trans ‐Hydrostannation of Boron‐Capped Alkynes

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Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes

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Other Objects (12)

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

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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

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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

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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

An Efficient and Scalable “Second Generation” Total Synthesis of the Marine Polyketide Limaol Endowed with Antiparasitic Activity

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

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An Efficient and Scalable “Second Generation” Total Synthesis of the Marine Polyketide Limaol Endowed with Antiparasitic Activity

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