α‐Amidoaldehydes as Substrates in Rhodium‐Catalyzed Intermolecular Alkyne Hydroacylation: The Synthesis of α‐Amidoketones

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: α‐Amidoaldehydes as Substrates in Rhodium‐Catalyzed Intermolecular Alkyne Hydroacylation: The Synthesis of α‐Amidoketones ; volume:26 ; number:51 ; year:2020 ; pages:11710-11714 ; extent:5
Chemistry - a European journal ; 26, Heft 51 (2020), 11710-11714 (gesamt 5)

Creator: Pal, Ritashree
O'Brien, Sean C.
Willis, Michael J.

DOI: 10.1002/chem.202002478

URN: urn:nbn:de:101:1-2022060516311457825534

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

Last update: 15.08.2025, 7:27 AM CEST

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Pal, Ritashree
O'Brien, Sean C.
Willis, Michael J.

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Rhodium-Catalyzed Enantioselective Desymmetrization

Rhodium-Catalyzed Macrocyclization of Peptides

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Rhodium-Catalyzed Asymmetric Arylation of Diarylmethylamines

Rhodium-Catalyzed Enantioselective Hydroacylation of Ketones

Asymmetric Rhodium-Catalyzed [4+3] Cycloaddition

Rhodium-Catalyzed Enantioselective Hydroamination of Allenes

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Rhodium-catalyzed intra- and intermolecular alkene hydroacylation : = Rhodium-katalisierte Intra- und Intermolecular Alken Hydroacylation

Rhodium-Catalyzed Enantioselective Desymmetrization

Rhodium-Catalyzed Macrocyclization of Peptides

Rhodium-Catalyzed Asymmetric Transfer Hydrogenation

Rhodium-Catalyzed Asymmetric Arylation of Diarylmethylamines

Rhodium-Catalyzed Enantioselective Hydroacylation of Ketones

Asymmetric Rhodium-Catalyzed [4+3] Cycloaddition

Rhodium-Catalyzed Enantioselective Hydroamination of Allenes

Rhodium‐Catalyzed Regioselective 3‐Fluoroallylic Cyanation

Rhodium‐Catalyzed Chemo‐, Regio‐, Diastereo‐, and Enantioselective Intermolecular (2+2+2) Cycloaddition of Three Unsymmetric 2π Components

Rhodium-Catalyzed Diastereoselective Intermolecular C-H Amination

Hochschulschrift

Rhodium-catalyzed intra- and intermolecular alkene hydroacylation : = Rhodium-katalisierte Intra- und Intermolecular Alken Hydroacylation

Rhodium-Catalyzed Enantioselective Desymmetrization

Rhodium-Catalyzed Macrocyclization of Peptides

Rhodium-Catalyzed Asymmetric Transfer Hydrogenation

Rhodium-Catalyzed Asymmetric Arylation of Diarylmethylamines

Rhodium-Catalyzed Enantioselective Hydroacylation of Ketones

Asymmetric Rhodium-Catalyzed [4+3] Cycloaddition

Rhodium-Catalyzed Enantioselective Hydroamination of Allenes

Rhodium‐Catalyzed Regioselective 3‐Fluoroallylic Cyanation

Rhodium‐Catalyzed Chemo‐, Regio‐, Diastereo‐, and Enantioselective Intermolecular (2+2+2) Cycloaddition of Three Unsymmetric 2π Components

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α‐Amidoaldehydes as Substrates in Rhodium‐Catalyzed Intermolecular Alkyne Hydroacylation: The Synthesis of α‐Amidoketones

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Other Objects (12)

Rhodium-Catalyzed Diastereoselective Intermolecular C-H Amination

Rhodium-catalyzed intra- and intermolecular alkene hydroacylation : = Rhodium-katalisierte Intra- und Intermolecular Alken Hydroacylation

Rhodium-Catalyzed Enantioselective Desymmetrization

Rhodium-Catalyzed Macrocyclization of Peptides

Rhodium-Catalyzed Asymmetric Transfer Hydrogenation

Rhodium-Catalyzed Asymmetric Arylation of Diarylmethylamines

Rhodium-Catalyzed Enantioselective Hydroacylation of Ketones

Asymmetric Rhodium-Catalyzed [4+3] Cycloaddition

Rhodium-Catalyzed Enantioselective Hydroamination of Allenes

Rhodium‐Catalyzed Regioselective 3‐Fluoroallylic Cyanation

Rhodium‐Catalyzed Chemo‐, Regio‐, Diastereo‐, and Enantioselective Intermolecular (2+2+2) Cycloaddition of Three Unsymmetric 2π Components

Rhodium‐Catalyzed Chemo‐, Regio‐, Diastereo‐, and Enantioselective Intermolecular (2+2+2) Cycloaddition of Three Unsymmetric 2π Components

Rhodium-Catalyzed Diastereoselective Intermolecular C-H Amination

Rhodium-catalyzed intra- and intermolecular alkene hydroacylation : = Rhodium-katalisierte Intra- und Intermolecular Alken Hydroacylation

Rhodium-Catalyzed Enantioselective Desymmetrization

Rhodium-Catalyzed Macrocyclization of Peptides

Rhodium-Catalyzed Asymmetric Transfer Hydrogenation

Rhodium-Catalyzed Asymmetric Arylation of Diarylmethylamines

Rhodium-Catalyzed Enantioselective Hydroacylation of Ketones

Asymmetric Rhodium-Catalyzed [4+3] Cycloaddition

Rhodium-Catalyzed Enantioselective Hydroamination of Allenes

Rhodium‐Catalyzed Regioselective 3‐Fluoroallylic Cyanation

Rhodium‐Catalyzed Chemo‐, Regio‐, Diastereo‐, and Enantioselective Intermolecular (2+2+2) Cycloaddition of Three Unsymmetric 2π Components

Rhodium‐Catalyzed Chemo‐, Regio‐, Diastereo‐, and Enantioselective Intermolecular (2+2+2) Cycloaddition of Three Unsymmetric 2π Components

Rhodium-Catalyzed Diastereoselective Intermolecular C-H Amination

Rhodium-catalyzed intra- and intermolecular alkene hydroacylation : = Rhodium-katalisierte Intra- und Intermolecular Alken Hydroacylation

Rhodium-Catalyzed Enantioselective Desymmetrization

Rhodium-Catalyzed Macrocyclization of Peptides

Rhodium-Catalyzed Asymmetric Transfer Hydrogenation

Rhodium-Catalyzed Asymmetric Arylation of Diarylmethylamines

Rhodium-Catalyzed Enantioselective Hydroacylation of Ketones

Asymmetric Rhodium-Catalyzed [4+3] Cycloaddition

Rhodium-Catalyzed Enantioselective Hydroamination of Allenes

Rhodium‐Catalyzed Regioselective 3‐Fluoroallylic Cyanation

Rhodium‐Catalyzed Chemo‐, Regio‐, Diastereo‐, and Enantioselective Intermolecular (2+2+2) Cycloaddition of Three Unsymmetric 2π Components

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