- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Transition Metal‐free Selenium‐mediated Aryl Amines via Reduction of Nitroarenes ; day:26 ; month:06 ; year:2023 ; extent:9
ChemSusChem ; (26.06.2023) (gesamt 9)
- Creator
-
Capperucci, Antonella
Clemente, Martina
Cenni, Alessio
Tanini, Damiano
- DOI
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10.1002/cssc.202300086
- URN
-
urn:nbn:de:101:1-2023062715053016956449
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:47 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
- Capperucci, Antonella
- Clemente, Martina
- Cenni, Alessio
- Tanini, Damiano
Other Objects (12)
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Metal‐Free Aryl Cross‐Coupling Directed by Traceless Linkers †
Metal‐Free Radical Borylation of Alkyl and Aryl Iodides
Continuous-flow synthesis of primary amines: Metal-free reduction of aliphatic and aromatic nitro derivatives with trichlorosilane
Metal-Free Reduction of Aromatic Nitro Compounds
Earth-Abundant Metal-Catalyzed and Transition Metal-Free Borylation of Aryl Halides
Metal-free synthesis of biarenes via photoextrusion in di(tri)aryl phosphates
Photo‐Induced Carbonylation of Aryl Bromides for the Synthesis of Aryl Esters and Amides Under Transition Metal‐Free Conditions
Metal‐Free Electrocatalysts for Oxygen Reduction to Hydrogen Peroxide
2D, Metal‐Free Electrocatalysts for the Nitrogen Reduction Reaction
Metal-free electrochemical synthesis of sulfonamides directly from (hetero)arenes, SO2, and amines
Catalysed Aryl Amine Syntheses via Azides: From Azidation of Aryl Halides to Azide Reduction and Direct Amination
Metal‐Free Radical Borylation of Alkyl and Aryl Iodides
Metal‐Free Aryl Cross‐Coupling Directed by Traceless Linkers †
Metal‐Free Radical Borylation of Alkyl and Aryl Iodides
Continuous-flow synthesis of primary amines: Metal-free reduction of aliphatic and aromatic nitro derivatives with trichlorosilane
Metal-Free Reduction of Aromatic Nitro Compounds
Earth-Abundant Metal-Catalyzed and Transition Metal-Free Borylation of Aryl Halides
Metal-free synthesis of biarenes via photoextrusion in di(tri)aryl phosphates
Photo‐Induced Carbonylation of Aryl Bromides for the Synthesis of Aryl Esters and Amides Under Transition Metal‐Free Conditions
Metal‐Free Electrocatalysts for Oxygen Reduction to Hydrogen Peroxide
2D, Metal‐Free Electrocatalysts for the Nitrogen Reduction Reaction
Metal-free electrochemical synthesis of sulfonamides directly from (hetero)arenes, SO2, and amines
Catalysed Aryl Amine Syntheses via Azides: From Azidation of Aryl Halides to Azide Reduction and Direct Amination
Metal‐Free Radical Borylation of Alkyl and Aryl Iodides
Metal‐Free Aryl Cross‐Coupling Directed by Traceless Linkers †
Metal‐Free Radical Borylation of Alkyl and Aryl Iodides
Continuous-flow synthesis of primary amines: Metal-free reduction of aliphatic and aromatic nitro derivatives with trichlorosilane
Metal-Free Reduction of Aromatic Nitro Compounds
Earth-Abundant Metal-Catalyzed and Transition Metal-Free Borylation of Aryl Halides
Metal-free synthesis of biarenes via photoextrusion in di(tri)aryl phosphates
Photo‐Induced Carbonylation of Aryl Bromides for the Synthesis of Aryl Esters and Amides Under Transition Metal‐Free Conditions
Metal‐Free Electrocatalysts for Oxygen Reduction to Hydrogen Peroxide
2D, Metal‐Free Electrocatalysts for the Nitrogen Reduction Reaction