Back to Search
Start Over
Metal-free oxidative decarbonylative coupling of aromatic aldehydes with arenes: direct access to biaryls
- Source :
- Chemical Communications. 51:5925-5928
- Publication Year :
- 2015
- Publisher :
- Royal Society of Chemistry (RSC), 2015.
-
Abstract
- A metal-free oxidative decarbonylative coupling of aromatic aldehydes with electron-rich or electron-deficient arenes to produce biaryl compounds was developed. This novel coupling was proposed to proceed via a non-chain radical homolytic aromatic substitution (HAS) type mechanism, based on the substrate scope, ortho-regioselectivity, radical trapping experiments and DFT calculation studies. With the ready availability of aromatic aldehydes and arenes, metal-free conditions should make this coupling attractive for the biaryl synthesis.
- Subjects :
- Aldehydes
Macrocyclic Compounds
Free Radicals
Oxidative Coupling
Radical trapping
Chemistry
Metals and Alloys
Substrate (chemistry)
Electrons
Stereoisomerism
General Chemistry
Oxidative phosphorylation
Electrophilic aromatic substitution
Catalysis
Surfaces, Coatings and Films
Electronic, Optical and Magnetic Materials
Homolysis
Coupling (electronics)
Metal free
Materials Chemistry
Ceramics and Composites
Organic chemistry
Oxidation-Reduction
Subjects
Details
- ISSN :
- 1364548X and 13597345
- Volume :
- 51
- Database :
- OpenAIRE
- Journal :
- Chemical Communications
- Accession number :
- edsair.doi.dedup.....43439e0a73ce03633ef929c53b142b7f