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Volumn 14, Issue 35, 2008, Pages 10919-10922

Synthesis of diarylamines catalyzed by iron salts

Author keywords

Anilines; Arylation; Catalysis; Cross coupling; Iron

Indexed keywords

AMINES; ANILINE; AROMATIC COMPOUNDS; CATALYSIS; SALTS;

EID: 57149139029     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200802018     Document Type: Article
Times cited : (52)

References (62)
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    • For similar results obtained by Taillefer and co-workers in the intermolecular O-arylation of phenols, see: c N. Xia, M. Taillefer, Chem. Eur. J. 2008, 14, 6037
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    • It should be pointed out that under such conditions aryne-type intermediates seem to be involved, leading to the formation of mixtures L of regioisomers. See: D. Guo, H. Huang, J. Xu, H. Jiang, H. Liu, Org. Lett. 2008. 10, 4513
    • It should be pointed out that under such conditions aryne-type intermediates seem to be involved, leading to the formation of mixtures L of regioisomers. See: D. Guo, H. Huang, J. Xu, H. Jiang, H. Liu, Org. Lett. 2008. 10, 4513.
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    • 3 with 98% purity purchased from Merck was used in all experiments reported here.
    • 3 with 98% purity purchased from Merck was used in all experiments reported here.
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    • All attempts conducted with different aryl sources (aryl bromides, aryl chlorides, tosylates, triflates and trimethoxysilanes) were unsuccessful, and unreacted acetanilides were always recovered
    • All attempts conducted with different aryl sources (aryl bromides, aryl chlorides, tosylates, triflates and trimethoxysilanes) were unsuccessful, and unreacted acetanilides were always recovered.


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