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Volumn 47, Issue 3, 2008, Pages 586-588

Iron-catalyzed C-O cross-couplings of phenols with aryl iodides

Author keywords

Arylation; Catalysis; Cross coupling; Iron; Phenol

Indexed keywords

CATALYST ACTIVITY; COST EFFECTIVENESS; ETHERS; IRON; LIGANDS;

EID: 38949187989     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200704018     Document Type: Article
Times cited : (195)

References (65)
  • 2
    • 0033516914 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1999, 38, 2096-2152;
    • (1999) Angew. Chem. Int. Ed , vol.38 , pp. 2096-2152
  • 6
    • 0032538360 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1998, 37, 2704-2708;
    • (1998) Angew. Chem. Int. Ed , vol.37 , pp. 2704-2708
  • 8
    • 0032538485 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1998, 37, 2708-2714.
    • (1998) Angew. Chem. Int. Ed , vol.37 , pp. 2708-2714
  • 13
    • 33746283734 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 4321-4326.
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 4321-4326
  • 22
    • 33745694711 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 1276-1279;
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 1276-1279
  • 27
    • 4143116053 scopus 로고    scopus 로고
    • For general reviews, see: a
    • For general reviews, see: a) S. V. Ley, A. W. Thomas, Angew. Chem. 2003, 115, 5558-5607;
    • (2003) Angew. Chem , vol.115 , pp. 5558-5607
    • Ley, S.V.1    Thomas, A.W.2
  • 28
    • 0345708168 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 5400-5449;
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 5400-5449
  • 37
    • 4544294922 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 3955-3957;
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 3955-3957
  • 39
    • 17044409192 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 1654-1658;
    • (2005) Chem. Int. Ed , vol.44 , pp. 1654-1658
    • Angew1
  • 42
    • 33746216342 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 2938-2941;
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 2938-2941
  • 47
    • 34948835849 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 7293-7296;
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 7293-7296
  • 52
    • 4644283257 scopus 로고    scopus 로고
    • For selected iron-catalyzed reactions reported by our group, see: a
    • For selected iron-catalyzed reactions reported by our group, see: a) J. Legros, C. Bolm, Angew. Chem. 2003, 115, 5645-5647;
    • (2003) Angew. Chem , vol.115 , pp. 5645-5647
    • Legros, J.1    Bolm, C.2
  • 53
    • 0344845085 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 5487-5489;
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 5487-5489
  • 55
    • 4644283019 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 4225-4228;
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 4225-4228
  • 60
    • 36749002068 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 8862-8865.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 8862-8865
  • 61
    • 40949151717 scopus 로고    scopus 로고
    • 3 as base in several organic reactions, see: T. Flessner, S. Doye, J. Prakt. Chem. 1999, 341, 793-796.
    • 3 as base in several organic reactions, see: T. Flessner, S. Doye, J. Prakt. Chem. 1999, 341, 793-796.
  • 62
    • 40949151284 scopus 로고    scopus 로고
    • When the reaction was performed at lower temperature (110°C), diphenyl ether (3a) was obtained in much lower yields.
    • When the reaction was performed at lower temperature (110°C), diphenyl ether (3a) was obtained in much lower yields.
  • 63
    • 40949141143 scopus 로고    scopus 로고
    • 3 (purity > 98 %) provided by Merck.
    • 3 (purity > 98 %) provided by Merck.
  • 64
    • 40949163586 scopus 로고    scopus 로고
    • 4-Nitrophenol has been shown to be unreactive in several copper-catalyzed O-arylation reactions with aryl halides. See reference [5g] and references cited therein.
    • 4-Nitrophenol has been shown to be unreactive in several copper-catalyzed O-arylation reactions with aryl halides. See reference [5g] and references cited therein.
  • 65
    • 40949137540 scopus 로고    scopus 로고
    • 3 and 40 mol % L3), no significant improvement was achieved, and the corresponding O-arylated product was obtained in 59 % yield after 20 h.
    • 3 and 40 mol % L3), no significant improvement was achieved, and the corresponding O-arylated product was obtained in 59 % yield after 20 h.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.