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Volumn 129, Issue 41, 2007, Pages 12404-12405

Copper-catalyzed arylation of heterocycle C-H bonds

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; COPPER; HETEROCYCLIC COMPOUND; HYDROGEN;

EID: 35348998959     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja075802+     Document Type: Article
Times cited : (485)

References (34)
  • 20
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    • 2). The cost of the copper-catalyzed reaction is $150 (iodobenzene) + $3 (CuI; Aldrich prices). An expensive ligand is usually used for palladium-catalyzed reactions.
    • 2). The cost of the copper-catalyzed reaction is $150 (iodobenzene) + $3 (CuI; Aldrich prices). An expensive ligand is usually used for palladium-catalyzed reactions.
  • 25
    • 33744786786 scopus 로고    scopus 로고
    • Cu-catalyzed oxidation of C-H bonds in 2-phenylpyridines: (a) Chen, X.; Hao, X.-S.; Goodhue, C. E.; Yu, J.-Q. J. Am. Chem. Soc. 2006, 128, 6790.
    • Cu-catalyzed oxidation of C-H bonds in 2-phenylpyridines: (a) Chen, X.; Hao, X.-S.; Goodhue, C. E.; Yu, J.-Q. J. Am. Chem. Soc. 2006, 128, 6790.
  • 27
    • 18744386111 scopus 로고    scopus 로고
    • Cu-catalyzed reaction of indoles with tetrahydroisoquinolines: (c) Li, Z.; Li, C.-J. J. Am. Chem. Soc. 2005, 127, 6968.
    • Cu-catalyzed reaction of indoles with tetrahydroisoquinolines: (c) Li, Z.; Li, C.-J. J. Am. Chem. Soc. 2005, 127, 6968.
  • 28
    • 0001568295 scopus 로고    scopus 로고
    • Heterocycle arylation under Pd, by Pd/Cu catalysis, or by using several equivalents of Cu: Pivsa-Art, S.; Satoh, T.; Kawamura, Y.; Miura, M.; Nomura, M. Bull. Chem. Soc. Jpn. 1998, 71, 467.
    • Heterocycle arylation under Pd, by Pd/Cu catalysis, or by using several equivalents of Cu: Pivsa-Art, S.; Satoh, T.; Kawamura, Y.; Miura, M.; Nomura, M. Bull. Chem. Soc. Jpn. 1998, 71, 467.
  • 29
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    • Palladium-catalyzed pyridine oxide arylation: Campeau, L.-C.; Rousseaux, S.; Fagnou, K. J. Am. Chem. Soc. 2005, 127, 18020.
    • Palladium-catalyzed pyridine oxide arylation: Campeau, L.-C.; Rousseaux, S.; Fagnou, K. J. Am. Chem. Soc. 2005, 127, 18020.
  • 30
    • 33947333803 scopus 로고    scopus 로고
    • Silver-benzyne complex reactions with arene nucleophiles: (a) Friedman, L. J. Am. Chem. Soc. 1967, 89, 3071.
    • Silver-benzyne complex reactions with arene nucleophiles: (a) Friedman, L. J. Am. Chem. Soc. 1967, 89, 3071.
  • 31
    • 0345329013 scopus 로고    scopus 로고
    • Review about Cu-catalyzed nucleophilic substitution: (b) Lindley, J. Tetrahedron 1984, 40, 1433.
    • Review about Cu-catalyzed nucleophilic substitution: (b) Lindley, J. Tetrahedron 1984, 40, 1433.
  • 32
    • 0037415520 scopus 로고    scopus 로고
    • Aryne substitution: (c) Pellissier, H.; Santelli, M. Tetrahedron 2003, 59, 701.
    • Aryne substitution: (c) Pellissier, H.; Santelli, M. Tetrahedron 2003, 59, 701.
  • 33
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    • Benzyne reactions with Pd species: (d) Liu, Z.; Larock, R. C. J. Org. Chem. 2007, 72, 223.
    • Benzyne reactions with Pd species: (d) Liu, Z.; Larock, R. C. J. Org. Chem. 2007, 72, 223.
  • 34
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    • Arylation of 4,5-dimethylthiazole by p-tolyl bromide under conditions of Scheme IA affords a mixture of m-tolyl- and p-tolylderivatives. See Supporting Information for details.
    • Arylation of 4,5-dimethylthiazole by p-tolyl bromide under conditions of Scheme IA affords a mixture of m-tolyl- and p-tolylderivatives. See Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.