Regioselective trans ‐Hydrostannation of Boron‐Capped Alkynes

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Regioselective trans ‐Hydrostannation of Boron‐Capped Alkynes ; day:04 ; month:08 ; year:2021 ; extent:1
Chemistry - a European journal ; (04.08.2021) (gesamt 1)

Creator: Melot, Romain
Saiegh, Tomas J.
Fürstner, Alois

DOI: 10.1002/chem.202101901

URN: urn:nbn:de:101:1-2021080415175888302510

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

Last update: 14.08.2025, 10:56 AM CEST

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Melot, Romain
Saiegh, Tomas J.
Fürstner, Alois

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Regioselective trans ‐Hydrostannation of Boron‐Capped Alkynes

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Other Objects (12)

How to Break the Law: trans ‐Hydroboration and gem ‐Hydroboration of Alkynes

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

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

SYNTHESIS Special Issue in Honor of Professor Sarah Reisman

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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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A Heteroleptic Dirhodium Catalyst for Asymmetric Cyclopropanation with α‐Stannyl α‐Diazoacetate. “Stereoretentive” Stille Coupling with Formation of Chiral Quarternary Carbon Centers

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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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Modular Synthesis of Furans with up to Four Different Substituents by a trans ‐Carboboration Strategy

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

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A Heteroleptic Dirhodium Catalyst for Asymmetric Cyclopropanation with α‐Stannyl α‐Diazoacetate. “Stereoretentive” Stille Coupling with Formation of Chiral Quarternary Carbon Centers

Total Synthesis of Mycinamicin IV as Integral Part of a Collective Approach to Macrolide Antibiotics

Scalable De Novo Synthesis of Aldgarose and Total Synthesis of Aldgamycin N

A Heteroleptic Dirhodium Catalyst for Asymmetric Cyclopropanation with α‐Stannyl α‐Diazoacetate. “Stereoretentive” Stille Coupling with Formation of Chiral Quarternary Carbon Centers

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

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

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

SYNTHESIS Special Issue in Honor of Professor Sarah Reisman

Modular Synthesis of Furans with up to Four Different Substituents by a trans ‐Carboboration Strategy

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

A Heteroleptic Dirhodium Catalyst for Asymmetric Cyclopropanation with α‐Stannyl α‐Diazoacetate. “Stereoretentive” Stille Coupling with Formation of Chiral Quarternary Carbon Centers

Total Synthesis of Mycinamicin IV as Integral Part of a Collective Approach to Macrolide Antibiotics

Scalable De Novo Synthesis of Aldgarose and Total Synthesis of Aldgamycin N

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