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Volumn 10, Issue 12, 2004, Pages 2983-2990

New ligands for a general palladium-catalyzed amination of aryl and heteroaryl chlorides

Author keywords

Amination; Anilines; Aryl chlorides; Catalysis; Palladium; Phosphines

Indexed keywords

AMINATION; CATALYSIS; CATALYSTS; PALLADIUM; QUENCHING; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

EID: 3042819291     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200306026     Document Type: Article
Times cited : (279)

References (69)
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    • Recent examples of Buchwald-Hartwig amination reactions: Buchwald group: a) D. Zim, S. L. Buchwald, Org. Lett. 2003, 5, 2413;
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    • Roy and Hartwig have shown that reductive elimination of aryl chlorides is slower than that of aryl bromides and aryl iodides see: A. H. Roy, J. F. Hartwig, J. Am. Chem. Soc. 2003, 125, 13 944.
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    • b) for an excellent review on palladium-catalyzed functionalizations of aryl chloride see: A. F. Littke, G. C. Fu, Angew. Chem. 2002, 114, 4350; Angew. Chem. Int. Ed. 2002, 41, 4176.
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    • 0037112673 scopus 로고    scopus 로고
    • b) for an excellent review on palladium-catalyzed functionalizations of aryl chloride see: A. F. Littke, G. C. Fu, Angew. Chem. 2002, 114, 4350; Angew. Chem. Int. Ed. 2002, 41, 4176.
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    • This ligand is now commercially available by Strem and Degussa Homogeneous Catalysts under the tradename cataCXium® A. For other applications see: a) A. Zapf, A. Ehrentraut, M. Beller, Angew. Chem. 2000, 112, 4315; Angew. Chem. Int. Ed. 2000, 39, 4153;
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    • This ligand is now commercially available by Strem and Degussa Homogeneous Catalysts under the tradename cataCXium® A. For other applications see: a) A. Zapf, A. Ehrentraut, M. Beller, Angew. Chem. 2000, 112, 4315; Angew. Chem. Int. Ed. 2000, 39, 4153;
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.