Attributes | Values |
---|
rdf:type
| |
description
| - wetenschappelijk artikel (nl)
- article scientifique (publié 2009) (fr)
- наукова стаття, опублікована в січні 2009 (uk)
- artículu científicu espublizáu en xineru de 2009 (ast)
- artikull shkencor i botuar më 01 janar 2009 (sq)
- scientific article published on 01 January 2009 (en)
|
publication date
| |
publication date
| |
cites work
| |
cites work
| - Click-Chemie: diverse chemische Funktionalität mit einer Handvoll guter Reaktionen
- Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(i)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides
- A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
- Polytriazoles as copper(I)-stabilizing ligands in catalysis
- Heterogeneous copper catalyst for the cycloaddition of azides and alkynes without additives under ambient conditions
- A microwave-assisted click chemistry synthesis of 1,4-disubstituted 1,2,3-triazoles via a copper(I)-catalyzed three-component reaction
- Ruthenium-catalyzed cycloaddition of alkynes and organic azides
- Rapid assembly and in situ screening of bidentate inhibitors of protein tyrosine phosphatases
- The growing impact of click chemistry on drug discovery
- Click chemistry in CuI-zeolites: the Huisgen [3 + 2]-cycloaddition
- Triazole-Linked Analogue of Deoxyribonucleic Acid (TLDNA): Design, Synthesis, and Double-Strand Formation with Natural DNA
- "Click" dendrimers: synthesis, redox sensing of Pd(OAc)2, and remarkable catalytic hydrogenation activity of precise Pd nanoparticles stabilized by 1,2,3-triazole-containing dendrimers
- Synthesis of neoglycopolymers by a combination of "click chemistry" and living radical polymerization
- A highly active and reusable copper(I)-tren catalyst for the "click" 1,3-dipolar cycloaddition of azides and alkynes
- "Click" chemistry in a supramolecular environment: stabilization of organogels by copper(I)-catalyzed azide-alkyne [3 + 2] cycloaddition.
- (NHC)Copper(I)-Catalyzed [3+2] Cycloaddition of Azides and Mono- or Disubstituted Alkynes
- Efficient oxidative alkyne homocoupling catalyzed by a monomeric dicopper-substituted silicotungstate.
- Heterogeneous copper-in-charcoal-catalyzed click chemistry.
- Click Chemistry: Copper Clusters Catalyse the Cycloaddition of Azides with Terminal Alkynes
- 1,3-Dipolar cycloaddition of organic azides to alkynes by a dicopper-substituted silicotungstate
- "Click chemistry" in zeolites: copper(I) zeolites as new heterogeneous and ligand-free catalysts for the Huisgen [3+2] cycloaddition
- One-pot procedure for diazo transfer and azide-alkyne cycloaddition: triazole linkages from amines
- Supported ruthenium catalyst for the heterogeneous oxidation of alcohols with molecular oxygen
- Synthesis of 5-(1,2,3-triazol-4-yl)-2'-deoxyuridines by a click chemistry approach: stacking of triazoles in the major groove gives increased nucleic acid duplex stability.
- Click-connected ligand scaffolds: macrocyclic chelates for asymmetric hydrogenation
- A one-pot synthesis of primary amides from aldoximes or aldehydes in water in the presence of a supported rhodium catalyst.
|
author name string
| |
author name string
| - Noritaka Mizuno
- Tatsuyori Katayama
|
rdfs:label
| - A supported copper hydroxide as an efficient, ligand-free, and heterogeneous precatalyst for 1,3-dipolar cycloadditions of organic azides to terminal alkynes (en)
- A supported copper hydroxide as an efficient, ligand-free, and heterogeneous precatalyst for 1,3-dipolar cycloadditions of organic azides to terminal alkynes (nl)
- A supported copper hydroxide as an efficient, ligand-free, and heterogeneous precatalyst for 1,3-dipolar cycloadditions of organic azides to terminal alkynes (sq)
|
skos:prefLabel
| - A supported copper hydroxide as an efficient, ligand-free, and heterogeneous precatalyst for 1,3-dipolar cycloadditions of organic azides to terminal alkynes (en)
- A supported copper hydroxide as an efficient, ligand-free, and heterogeneous precatalyst for 1,3-dipolar cycloadditions of organic azides to terminal alkynes (nl)
- A supported copper hydroxide as an efficient, ligand-free, and heterogeneous precatalyst for 1,3-dipolar cycloadditions of organic azides to terminal alkynes (sq)
|
name
| - A supported copper hydroxide as an efficient, ligand-free, and heterogeneous precatalyst for 1,3-dipolar cycloadditions of organic azides to terminal alkynes (en)
- A supported copper hydroxide as an efficient, ligand-free, and heterogeneous precatalyst for 1,3-dipolar cycloadditions of organic azides to terminal alkynes (nl)
- A supported copper hydroxide as an efficient, ligand-free, and heterogeneous precatalyst for 1,3-dipolar cycloadditions of organic azides to terminal alkynes (sq)
|
author
| |
author
| |
title
| |
title
| - A supported copper hydroxide as an efficient, ligand-free, and heterogeneous precatalyst for 1,3-dipolar cycloadditions of organic azides to terminal alkynes (en)
|
page(s)
| |
page(s)
| |
instance of
| |
instance of
| |
main subject
| |
main subject
| |
PubMed ID
| |
PubMed ID
| |
PubMed ID
| |
published in
| |
published in
| |
issue
| |
volume
| |
issue
| |
volume
| |
DOI
| |
DOI
| |
DOI
| |
is about
of | |