articleTop 1% cited
Copper-Catalyzed “Click” Reaction/Direct Arylation Sequence: Modular Syntheses of 1,2,3-Triazoles
Organic Letters · 2008 · Vol. 10(14) · pp. 3081–3084
Lutz Ackermann✉(University of Göttingen)Harish K. Potukuchi(University of Göttingen)Dirk Landsberg(University of Göttingen)R. Vicente(University of Göttingen)
Abstract
Inexpensive copper catalysts enabled modular one-pot multicomponent syntheses of fully decorated triazoles through a sustainable "click" reaction/direct arylation sequence.
Click Chemistry and ApplicationsChemical Synthesis and AnalysisCatalytic Cross-Coupling ReactionsChemistryCatalysisSequence (biology)Modular designCombinatorial chemistryCopperClick chemistryTriazoleCycloadditionOrganic chemistry
MeSH terms
CatalysisCopperTriazolesMolecular StructureCombinatorial Chemistry Techniques
Funding
- Deutscher Akademischer Austauschdienst
Citations
344
FWCI
16.52
field-weighted impact
References
40
Percentile
100%
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Citations per year
Cited by
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References
Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides
The Journal of Organic Chemistry · 2002 · 8,416 citations
Assisted Ruthenium-Catalyzed C−H Bond Activation: Carboxylic Acids as Cocatalysts for Generally Applicable Direct Arylations in Apolar Solvents
Organic Letters · 2008 · 391 citations
The growing applications of click chemistry
Chemical Society Reviews · 2007 · 2,325 citations
A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes
Angewandte Chemie International Edition · 2002 · 11,380 citations
1.3‐Dipolare Cycloadditionen Rückschau und Ausblick
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