- 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
-
Iron‐Mediated Electrophilic Amination of Organozinc Halides using Organic Azides ; volume:59 ; number:1 ; year:2020 ; pages:335-338 ; extent:4
Angewandte Chemie / International edition. International edition ; 59, Heft 1 (2020), 335-338 (gesamt 4)
- Creator
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Graßl, Simon
Singer, Johannes
Knochel, Paul
- DOI
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10.1002/anie.201911704
- URN
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urn:nbn:de:101:1-2022052707263395112841
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:32 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
- Graßl, Simon
- Singer, Johannes
- Knochel, Paul
Other Objects (12)
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Elaboration of electrophilic carbon heteroatom bond forming reactions using organozinc reagents
Regioselective C–H Activation of Substituted Pyridines and other Azines using Mg- and Zn-TMP-Bases
Recent Advances of the Halogen–Zinc Exchange Reaction
Iron-, Cobalt- and Chromium-catalyzed cross-coupling reactions of aromatics and heterocycles
Stereoselective preparation of chiral secondary alkylcopper- and zinc reagents. Subsequent reactions with allylic substrates and palladium-catalyzed cross-couplings with alkenyl and aryl halides
Cobalt-, iron-, and nickel-catalyzed cross-coupling reactions of zinc and manganese organometallics
Generation of aryl and heteroaryl magnesium and zinc reagents in toluene by Br/Mg and I/Zn exchange reactions and new iron-catalyzed cross-couplings of organomanganese species
Highly Regioselective Addition of Allylic Zinc Halides and Various Zinc Enolates to (1.1.1) Propellane
Iron‐Catalyzed Radical Zincations of Alkyl Iodides
Metalation and amination of N-heterocycles and the halogen/zinc exchange of aryl halides
Preface – Special Issue Dedicated to Professor Herbert Mayr
Natural Products in the Chemical Industry
Elaboration of electrophilic carbon heteroatom bond forming reactions using organozinc reagents
Regioselective C–H Activation of Substituted Pyridines and other Azines using Mg- and Zn-TMP-Bases
Recent Advances of the Halogen–Zinc Exchange Reaction
Iron-, Cobalt- and Chromium-catalyzed cross-coupling reactions of aromatics and heterocycles
Stereoselective preparation of chiral secondary alkylcopper- and zinc reagents. Subsequent reactions with allylic substrates and palladium-catalyzed cross-couplings with alkenyl and aryl halides
Cobalt-, iron-, and nickel-catalyzed cross-coupling reactions of zinc and manganese organometallics
Generation of aryl and heteroaryl magnesium and zinc reagents in toluene by Br/Mg and I/Zn exchange reactions and new iron-catalyzed cross-couplings of organomanganese species
Highly Regioselective Addition of Allylic Zinc Halides and Various Zinc Enolates to (1.1.1) Propellane
Iron‐Catalyzed Radical Zincations of Alkyl Iodides
Metalation and amination of N-heterocycles and the halogen/zinc exchange of aryl halides
Preface – Special Issue Dedicated to Professor Herbert Mayr
Natural Products in the Chemical Industry
Elaboration of electrophilic carbon heteroatom bond forming reactions using organozinc reagents
Regioselective C–H Activation of Substituted Pyridines and other Azines using Mg- and Zn-TMP-Bases
Recent Advances of the Halogen–Zinc Exchange Reaction
Iron-, Cobalt- and Chromium-catalyzed cross-coupling reactions of aromatics and heterocycles
Stereoselective preparation of chiral secondary alkylcopper- and zinc reagents. Subsequent reactions with allylic substrates and palladium-catalyzed cross-couplings with alkenyl and aryl halides
Cobalt-, iron-, and nickel-catalyzed cross-coupling reactions of zinc and manganese organometallics
Generation of aryl and heteroaryl magnesium and zinc reagents in toluene by Br/Mg and I/Zn exchange reactions and new iron-catalyzed cross-couplings of organomanganese species
Highly Regioselective Addition of Allylic Zinc Halides and Various Zinc Enolates to (1.1.1) Propellane