Copper(I)-catalyzed tandem reaction: synthesis of 1,4-disubstituted 1,2,3-triazoles from alkyl diacyl peroxides, azidotrimethylsilane, and alkynes
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Copper(I)-catalyzed tandem reaction: synthesis of 1,4-disubstituted 1,2,3-triazoles from alkyl diacyl peroxides, azidotrimethylsilane, and alkynes ; volume:14 ; pages:2916-2922
Beilstein journal of organic chemistry ; 14, 2916-2922
- Classification
-
Chemie
- DOI
-
10.3762/bjoc.14.270
- URN
-
urn:nbn:de:101:1-2019120509045259365825
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:49 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)
Disubstituted 1,2,3-triazoles : a multitool for biomolecular chemistry
Disubstituted 1,2,3-Triazoles: A Multitool for Biomolecular Chemistry
Synthesis of N-perfluoroalkyl-3,4-disubstituted pyrroles by rhodium-catalyzed transannulation of N-fluoroalkyl-1,2,3-triazoles with terminal alkynes
Synthesis of 2-tetrafluoropyridyl-4,5-disubstituted 1,2,3-triazoles
PEG-Supported Synthesis of 3,5-Disubstituted-1,2,4-Triazoles
Regio‐ and enantioselective nickel-alkyl catalyzed hydroalkylation of alkynes
Synthesis and crystal structural characterization of two new 3,5-disubstituted 4-amino-1,2,4-triazoles
Click triazoles
Gold‐Catalyzed One‐Pot Synthesis of 1,3‐Disubstituted Allenes from Benzaldehydes and Terminal Alkynes
Hydrosilylation of Alkynes Catalyzed by an Iron (II) PCP Pincer Alkyl Complex
Thermal properties and decomposition mechanism of disubstituted fused 1,2,4-triazoles considered as potential anticancer and antibacterial agents
[3+2] Cycloaddition of alkyl aldehydes and alkynes enabled by photoinduced hydrogen atom transfer
Disubstituted 1,2,3-triazoles : a multitool for biomolecular chemistry
Disubstituted 1,2,3-Triazoles: A Multitool for Biomolecular Chemistry
Synthesis of N-perfluoroalkyl-3,4-disubstituted pyrroles by rhodium-catalyzed transannulation of N-fluoroalkyl-1,2,3-triazoles with terminal alkynes
Synthesis of 2-tetrafluoropyridyl-4,5-disubstituted 1,2,3-triazoles
PEG-Supported Synthesis of 3,5-Disubstituted-1,2,4-Triazoles
Regio‐ and enantioselective nickel-alkyl catalyzed hydroalkylation of alkynes
Synthesis and crystal structural characterization of two new 3,5-disubstituted 4-amino-1,2,4-triazoles
Click triazoles
Gold‐Catalyzed One‐Pot Synthesis of 1,3‐Disubstituted Allenes from Benzaldehydes and Terminal Alkynes
Hydrosilylation of Alkynes Catalyzed by an Iron (II) PCP Pincer Alkyl Complex
Thermal properties and decomposition mechanism of disubstituted fused 1,2,4-triazoles considered as potential anticancer and antibacterial agents
[3+2] Cycloaddition of alkyl aldehydes and alkynes enabled by photoinduced hydrogen atom transfer
Disubstituted 1,2,3-triazoles : a multitool for biomolecular chemistry
Disubstituted 1,2,3-Triazoles: A Multitool for Biomolecular Chemistry
Synthesis of N-perfluoroalkyl-3,4-disubstituted pyrroles by rhodium-catalyzed transannulation of N-fluoroalkyl-1,2,3-triazoles with terminal alkynes
Synthesis of 2-tetrafluoropyridyl-4,5-disubstituted 1,2,3-triazoles
PEG-Supported Synthesis of 3,5-Disubstituted-1,2,4-Triazoles
Regio‐ and enantioselective nickel-alkyl catalyzed hydroalkylation of alkynes
Synthesis and crystal structural characterization of two new 3,5-disubstituted 4-amino-1,2,4-triazoles
Click triazoles
Gold‐Catalyzed One‐Pot Synthesis of 1,3‐Disubstituted Allenes from Benzaldehydes and Terminal Alkynes
Hydrosilylation of Alkynes Catalyzed by an Iron (II) PCP Pincer Alkyl Complex
Thermal properties and decomposition mechanism of disubstituted fused 1,2,4-triazoles considered as potential anticancer and antibacterial agents