Facilitating the Ferration of Aromatic Substrates through Intramolecular Sodium Mediation
- 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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Facilitating the Ferration of Aromatic Substrates through Intramolecular Sodium Mediation ; day:17 ; month:06 ; year:2021 ; extent:7
Angewandte Chemie ; (17.06.2021) (gesamt 7)
- Creator
- DOI
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10.1002/ange.202104275
- URN
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urn:nbn:de:101:1-2021062316480546649192
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:59 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Maddock, Lewis C. H.
- Mu, Manting
- Kennedy, Alan R.
- García-Melchor, Max
- Hevia, Eva
Other Objects (12)
Facilitating the Ferration of Aromatic Substrates through Intramolecular Sodium Mediation
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Development of hydrogen isotope exchange methodologies for the deuteration of aromatic substrates
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Complete σ* intramolecular aromatic hydroxylation mechanism through O2 activation by a Schiff base macrocyclic dicopper(I) complex
An unusual route to a quinoline 1-oxide via intramolecular addition of an enolate to an aromatic nitro group
Intramolecular carbonickelation of alkenes
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Room‐Temperature‐Observable Interconversion Between Si (IV) and Si (II) via Reversible Intramolecular Insertion Into an Aromatic C−C Bond
Bimetallic Nanoparticles in Supported Ionic Liquid Phases as Multifunctional Catalysts for the Selective Hydrodeoxygenation of Aromatic Substrates
Facilitating the Ferration of Aromatic Substrates through Intramolecular Sodium Mediation
Selective hydrodeoxygenation of carbonyl-substituted aromatic substrates using multifunctional catalysts
Nation-building and identity conflicts : facilitating the mediation process in Southern Philippines
Development of hydrogen isotope exchange methodologies for the deuteration of aromatic substrates
Intramolecular glycosylation
Complete σ* intramolecular aromatic hydroxylation mechanism through O2 activation by a Schiff base macrocyclic dicopper(I) complex
An unusual route to a quinoline 1-oxide via intramolecular addition of an enolate to an aromatic nitro group
Intramolecular carbonickelation of alkenes
Facilitating leadership decisions
Facilitating leadership decisions
Room‐Temperature‐Observable Interconversion Between Si (IV) and Si (II) via Reversible Intramolecular Insertion Into an Aromatic C−C Bond
Bimetallic Nanoparticles in Supported Ionic Liquid Phases as Multifunctional Catalysts for the Selective Hydrodeoxygenation of Aromatic Substrates
Facilitating the Ferration of Aromatic Substrates through Intramolecular Sodium Mediation
Selective hydrodeoxygenation of carbonyl-substituted aromatic substrates using multifunctional catalysts
Nation-building and identity conflicts : facilitating the mediation process in Southern Philippines
Development of hydrogen isotope exchange methodologies for the deuteration of aromatic substrates
Intramolecular glycosylation
Complete σ* intramolecular aromatic hydroxylation mechanism through O2 activation by a Schiff base macrocyclic dicopper(I) complex
An unusual route to a quinoline 1-oxide via intramolecular addition of an enolate to an aromatic nitro group
Intramolecular carbonickelation of alkenes
Facilitating leadership decisions
Facilitating leadership decisions
Room‐Temperature‐Observable Interconversion Between Si (IV) and Si (II) via Reversible Intramolecular Insertion Into an Aromatic C−C Bond