Universal Journal of Chemistry(CEASE PUBLICATION) Vol. 2(2), pp. 23 - 29
DOI: 10.13189/ujc.2014.020202
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Catalytic Activity of a Dimeric Palladacycle of 2-Phenylaniline in Suzuki and Heck Cross-coupling Reactions

Kazem Karami ^*, Zohreh Karami Moghadama , Mahboubeh Hosseini Kharata
Department of Chemistry, Isfahan University of Technology, Isfahan, 84156/83111, Iran

ABSTRACT

A dimeric NC-palladacycle of 2-phenylaniline was applied in the Suzuki reaction of aryl halides and the Heck reaction of methyl acrylate and styrene with phenylboronic acid. This palladacycle was found to be effective catalyst for the Suzuki and Heck cross-coupling reactions which could be carried out in the undried solvent under air.

KEYWORDS
NC-Palladacycle, Catalytic Activity, Suzuki Reaction, Heck Reaction, Promoter

Cite This Paper in IEEE or APA Citation Styles
(a). IEEE Format:
[1] Kazem Karami , Zohreh Karami Moghadama , Mahboubeh Hosseini Kharata , "Catalytic Activity of a Dimeric Palladacycle of 2-Phenylaniline in Suzuki and Heck Cross-coupling Reactions," Universal Journal of Chemistry(CEASE PUBLICATION), Vol. 2, No. 2, pp. 23 - 29, 2014. DOI: 10.13189/ujc.2014.020202.

(b). APA Format:
Kazem Karami , Zohreh Karami Moghadama , Mahboubeh Hosseini Kharata (2014). Catalytic Activity of a Dimeric Palladacycle of 2-Phenylaniline in Suzuki and Heck Cross-coupling Reactions. Universal Journal of Chemistry(CEASE PUBLICATION), 2(2), 23 - 29. DOI: 10.13189/ujc.2014.020202.