- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
-
The Azide‐Wittig Reaction ; day:09 ; month:11 ; year:2024 ; extent:8
Angewandte Chemie / International edition. International edition ; (09.11.2024) (gesamt 8)
- Creator
- DOI
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10.1002/anie.202412982
- URN
-
urn:nbn:de:101:1-2411101328113.520405062458
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:21 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
- Kushik
- Petrov, A.
- Ranieri, D.
- Edelmann, L.
- Beweries, Torsten
- Hering-Junghans, Christian
Other Objects (12)
Wittig Reaction
Recent Developments in the Ruthenium‐Catalyzed Azide Alkyne Cycloaddition (RuAAC) Reaction
p-Toluenesulfonyl Azide
Post‐Functionalization of Organoboranes by Cu‐Catalyzed Azide Alkyne (3+2)‐Cycloaddition Reaction
Transformation of Highly Hydrophobic Triarylphosphines into Amphiphiles via Staudinger Reaction with Hydrophilic Trichlorophenyl Azide
Imidazole-1-sulfonyl Azide Hydrochloride
Investigation of reactions involving pentacoordinate intermediates : the mechanism of the Wittig reaction
RuIII(edta) mediated oxidation of azide in the presence of hydrogen peroxide. Azide versus peroxide activation
Combining the Ugi-azide multicomponent reaction and rhodium(III)-catalyzed annulation for the synthesis of tetrazole-isoquinolone/pyridone hybrids
Exploration of the 1,3-dipolar cycloaddition reaction between azide and phosphorane partners and use in peptide ligation
Neue Azide und Azidokomplexe einiger Übergangsmetalle
Die Hydrazide und Azide der Phtalsäuren
Wittig Reaction
Recent Developments in the Ruthenium‐Catalyzed Azide Alkyne Cycloaddition (RuAAC) Reaction
p-Toluenesulfonyl Azide
Post‐Functionalization of Organoboranes by Cu‐Catalyzed Azide Alkyne (3+2)‐Cycloaddition Reaction
Transformation of Highly Hydrophobic Triarylphosphines into Amphiphiles via Staudinger Reaction with Hydrophilic Trichlorophenyl Azide
Imidazole-1-sulfonyl Azide Hydrochloride
Investigation of reactions involving pentacoordinate intermediates : the mechanism of the Wittig reaction
RuIII(edta) mediated oxidation of azide in the presence of hydrogen peroxide. Azide versus peroxide activation
Combining the Ugi-azide multicomponent reaction and rhodium(III)-catalyzed annulation for the synthesis of tetrazole-isoquinolone/pyridone hybrids
Exploration of the 1,3-dipolar cycloaddition reaction between azide and phosphorane partners and use in peptide ligation
Neue Azide und Azidokomplexe einiger Übergangsmetalle
Die Hydrazide und Azide der Phtalsäuren
Wittig Reaction
Recent Developments in the Ruthenium‐Catalyzed Azide Alkyne Cycloaddition (RuAAC) Reaction
p-Toluenesulfonyl Azide
Post‐Functionalization of Organoboranes by Cu‐Catalyzed Azide Alkyne (3+2)‐Cycloaddition Reaction
Transformation of Highly Hydrophobic Triarylphosphines into Amphiphiles via Staudinger Reaction with Hydrophilic Trichlorophenyl Azide
Imidazole-1-sulfonyl Azide Hydrochloride
Investigation of reactions involving pentacoordinate intermediates : the mechanism of the Wittig reaction
RuIII(edta) mediated oxidation of azide in the presence of hydrogen peroxide. Azide versus peroxide activation
Combining the Ugi-azide multicomponent reaction and rhodium(III)-catalyzed annulation for the synthesis of tetrazole-isoquinolone/pyridone hybrids
Exploration of the 1,3-dipolar cycloaddition reaction between azide and phosphorane partners and use in peptide ligation
Neue Azide und Azidokomplexe einiger Übergangsmetalle