An efficient heterogeneous ligand free C–N coupling reaction catalyzed by palladium supported on magnetic nanoparticles

[Display omitted] The catalytic activity of palladium supported on magnetic nanoparticles in the amination coupling reaction of different nitrogen containing substrates with aryl halides was investigated. C–N bond formation was achieved in moderate to excellent yields and the catalyst could be separ...

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Bibliographic Details
Published inTetrahedron letters Vol. 57; no. 2; pp. 219 - 222
Main Authors Rafiee, Ezzat, Ataei, Ali, Joshaghani, Mohammad
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier Ltd 13.01.2016
Elsevier
Subjects
Amination coupling
Catalyst
Chemistry
Chemistry, Organic
Magnetic nanoparticle
Palladium
Physical Sciences
Science & Technology
Triphenylamine
Magnetic nanoparticle
Amination coupling
Palladium
Triphenylamine
Catalyst
ORGANIC-SYNTHESIS
ROOM-TEMPERATURE
AROMATIC AMINATION
BROMIDES
AMINES
ARYL HALIDES
CHLORIDES
HECK REACTION
BOND
DERIVATIVES
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Summary:[Display omitted] The catalytic activity of palladium supported on magnetic nanoparticles in the amination coupling reaction of different nitrogen containing substrates with aryl halides was investigated. C–N bond formation was achieved in moderate to excellent yields and the catalyst could be separated by magnetic decantation.
ISSN:0040-4039
1873-3581
DOI:10.1016/j.tetlet.2015.12.020