Keywords
ChemistryBenzaldehydePalladiumCatalysisArylMedicinal chemistryOrganic chemistry
Affiliated Institutions
Related Publications
Superparamagnetic Nanoparticle-Supported Catalysis of Suzuki Cross-Coupling Reactions
Emulsion polymerization was examined as a novel route for the synthesis of core/shell superparamagnetic nanoparticles consisting of a highly crystalline gamma-Fe2O3 core and a v...
Pd Metal Catalysts for Cross-Couplings and Related Reactions in the 21st Century: A Critical Review
Cross-couplings and related reactions are a class of highly efficient synthetic protocols that are generally promoted by molecular Pd species as catalysts. However, catalysts ba...
Nucleophilic Degradation of Fenitrothion Insecticide and Performance of Nucleophiles: A Computational Study
Ab initio and density functional theory (DFT) calculations have been performed to understand the destruction chemistry of an important organophosphorus insecticide O,O-dimethyl ...
Preparation of Highly Conjugated Oligoaza-PAHs Based on the Oxidative Intramolecular Coupling of Bicyclo[2.2.2]octadiene-Fused Pyrrole
The substitution reactions of tetrafluoro-p-phthalonitrile and hexafluorobenzene with 4,7-dihydro-4,7-ethano-2H-isoindole under basic conditions afforded tetra(4,7-dihydro-4,7-e...
Photoredox functionalization of C–H bonds adjacent to a nitrogen atom
The functionalization of C-H bonds and the visible light photoredox catalysis represent two prominent challenges in organic chemistry. In this regard, the combination of visible...
Publication Info
- Year
- 2005
- Type
- article
- Volume
- 46
- Issue
- 13
- Pages
- 2273-2277
- Citations
- 130
- Access
- Closed
External Links
Social Impact
Altmetric
PlumX Metrics
Social media, news, blog, policy document mentions
Citation Metrics
130
OpenAlex
Cite This
Nevın Gürbüz,
İsmaıl Özdemır,
Bekır Çetınkaya
(2005).
Selective palladium-catalyzed arylation(s) of benzaldehyde derivatives by N-heterocarbene ligands.
Tetrahedron Letters
, 46
(13)
, 2273-2277.
https://doi.org/10.1016/j.tetlet.2005.02.023
Identifiers
- DOI
- 10.1016/j.tetlet.2005.02.023