Continuous-flow synthesis of primary amines: Metal-free reduction of aliphatic and aromatic nitro derivatives with trichlorosilane
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Continuous-flow synthesis of primary amines: Metal-free reduction of aliphatic and aromatic nitro derivatives with trichlorosilane ; volume:12 ; pages:2614-2619
Beilstein journal of organic chemistry ; 12, 2614-2619
- Classification
-
Chemie
- DOI
-
10.3762/bjoc.12.257
- URN
-
urn:nbn:de:101:1-2018090415290157356719
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:20 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.
Other Objects (12)
Regiospecific N‐Arylation of Aliphatic Amines under Mild and Metal‐Free Reaction Conditions
Regiospecific N‐Arylation of Aliphatic Amines under Mild and Metal‐Free Reaction Conditions
Room Temperature, Metal‐Free Arylation of Aliphatic Alcohols
Metal-Free Reduction of Aromatic Nitro Compounds
Aliphatic Amines Formed by Asymmetric Copper-Catalyzed Hydroamination
Aliphatic Amines Unlocked for Selective Transformations through Diazotization
Aliphatic Amines Unlocked for Selective Transformations through Diazotization
Cu‐Catalyzed Coupling of Aliphatic Amines with Alkylboronic Esters
Secondary aerosol formation from atmospheric reactions of aliphatic amines
The ozonolysis of primary aliphatic amines in fine particles
Palladium‐Catalyzed Hydroaminocarbonylation of Olefins with Aliphatic Amines without Additives
Unexpected Acetylation of Endogenous Aliphatic Amines by Arylamine N ‐Acetyltransferase NAT2
Regiospecific N‐Arylation of Aliphatic Amines under Mild and Metal‐Free Reaction Conditions
Regiospecific N‐Arylation of Aliphatic Amines under Mild and Metal‐Free Reaction Conditions
Room Temperature, Metal‐Free Arylation of Aliphatic Alcohols
Metal-Free Reduction of Aromatic Nitro Compounds
Aliphatic Amines Formed by Asymmetric Copper-Catalyzed Hydroamination
Aliphatic Amines Unlocked for Selective Transformations through Diazotization
Aliphatic Amines Unlocked for Selective Transformations through Diazotization
Cu‐Catalyzed Coupling of Aliphatic Amines with Alkylboronic Esters
Secondary aerosol formation from atmospheric reactions of aliphatic amines
The ozonolysis of primary aliphatic amines in fine particles
Palladium‐Catalyzed Hydroaminocarbonylation of Olefins with Aliphatic Amines without Additives
Unexpected Acetylation of Endogenous Aliphatic Amines by Arylamine N ‐Acetyltransferase NAT2
Regiospecific N‐Arylation of Aliphatic Amines under Mild and Metal‐Free Reaction Conditions
Regiospecific N‐Arylation of Aliphatic Amines under Mild and Metal‐Free Reaction Conditions
Room Temperature, Metal‐Free Arylation of Aliphatic Alcohols
Metal-Free Reduction of Aromatic Nitro Compounds
Aliphatic Amines Formed by Asymmetric Copper-Catalyzed Hydroamination
Aliphatic Amines Unlocked for Selective Transformations through Diazotization
Aliphatic Amines Unlocked for Selective Transformations through Diazotization
Cu‐Catalyzed Coupling of Aliphatic Amines with Alkylboronic Esters
Secondary aerosol formation from atmospheric reactions of aliphatic amines
The ozonolysis of primary aliphatic amines in fine particles
Palladium‐Catalyzed Hydroaminocarbonylation of Olefins with Aliphatic Amines without Additives