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Volumn 46, Issue 46, 2007, Pages 8862-8865

Iron-catalyzed N-arylation of nitrogen nucleophiles

Author keywords

Arylation; Cross coupling; Diamine ligands; Iron catalysis; Nitrogen heterocycles

Indexed keywords

AMIDES; CARBON DIOXIDE; CATALYSIS; IRON COMPOUNDS; LIGANDS; NITROGEN;

EID: 36749002068     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200703299     Document Type: Article
Times cited : (240)

References (46)
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    • For selected iron-catalyzed reactions reported by our research group, see: a
    • For selected iron-catalyzed reactions reported by our research group, see: a) J. Legros, C. Bolm, Angew. Chem. 2003, 115, 5645;
    • (2003) Angew. Chem , vol.115 , pp. 5645
    • Legros, J.1    Bolm, C.2
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    • 2O, a chiral diamine, and pyridine-2,6-dicarboxylic acid was used, see: F. G. Gelalcha, B. Bitterlich, G. Anilkumar, M. K. Tse, M. Beller, Angew. Chem. 2007, 119, 7431;
    • 2O, a chiral diamine, and pyridine-2,6-dicarboxylic acid was used, see: F. G. Gelalcha, B. Bitterlich, G. Anilkumar, M. K. Tse, M. Beller, Angew. Chem. 2007, 119, 7431;
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    • 3 was used.
    • 3 was used.
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    • 2, led to only trace amounts of N-phenyl pyrazole (3a).
    • 2, led to only trace amounts of N-phenyl pyrazole (3a).
  • 45
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    • An increase in the temperature from 110 to 135°C in method A resulted in lower yields of 3a than those observed with method B
    • An increase in the temperature from 110 to 135°C in method A resulted in lower yields of 3a than those observed with method B.
  • 46
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    • 3 (purity > 98 %) provided by Merck.
    • 3 (purity > 98 %) provided by Merck.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.