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Palladium-nanoparticle-catalyzed 1,7-palladium migration involving C-H activation, followed by intramolecular lamination: Regioselective synthesis of N 1-arylbenzotriazoles and an evaluation of their inhibitory activity toward indoleamine 2,3-dioxygenase
- Source :
- Journal of Organic Chemistry. 79(13):6366-6371
- Publication Year :
- 2014
- Publisher :
- American Chemical Society, 2014.
-
Abstract
- A sulfur-modified gold-supported palladium material (SAPd) has been developed bearing palladium nanoparticles on its surface. Herein, we report for the first time the use of SAPd to affect a Pd-nanoparticle-catalyzed 1,7-Pd migration reaction for the synthesis of benzotriazoles via C-H bond activation. The resulting benzotriazoles were evaluated in terms of their inhibitory activity toward indoleamine 2,3-dioxygenase.
- Subjects :
- inorganic chemicals
Molecular Structure
Stereochemistry
Organic Chemistry
chemistry.chemical_element
Nanoparticle
Regioselectivity
Triazoles
Inhibitory postsynaptic potential
Combinatorial chemistry
Catalysis
chemistry
Intramolecular force
Indoleamine-Pyrrole 2,3,-Dioxygenase
Nanoparticles
Enzyme Inhibitors
Indoleamine 2,3-dioxygenase
Amination
Palladium
Subjects
Details
- Language :
- English
- ISSN :
- 00223263
- Volume :
- 79
- Issue :
- 13
- Database :
- OpenAIRE
- Journal :
- Journal of Organic Chemistry
- Accession number :
- edsair.doi.dedup.....955d43aa64e7ea0c888394e8b2e07219