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Volumn 73, Issue 6, 2008, Pages 2476-2479

Synthesis of indole-3-carboxylic acid derivatives by Pd(0)-catalyzed intramolecular α-arylation of β-(2-iodoanilino) esters

Author keywords

[No Author keywords available]

Indexed keywords

ARYLATION; POTASSIUM PHENOXIDE;

EID: 41849116716     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800034m     Document Type: Article
Times cited : (56)

References (61)
  • 1
    • 0003979828 scopus 로고    scopus 로고
    • Academic Press: London
    • (a) Sundberg, R. J. Indoles; Academic Press: London, 1996.
    • (1996) Indoles
    • Sundberg, R.J.1
  • 2
    • 33751532464 scopus 로고    scopus 로고
    • George Thieme Verlag: Stuttgart
    • (b) Joule, J. A. In Science of Synthesis; George Thieme Verlag: Stuttgart 2000; Vol. 10.
    • (2000) Science of Synthesis , vol.10
    • Joule, J.A.1
  • 3
    • 34547095509 scopus 로고    scopus 로고
    • and previous reviews in these series
    • (c) Kazuhiro, H.; Kawassaki, T. Nat. Prod. Rep. 2007, 24, 843 and previous reviews in these series.
    • (2007) Nat. Prod. Rep , vol.24 , pp. 843
    • Kazuhiro, H.1    Kawassaki, T.2
  • 4
    • 22944454156 scopus 로고    scopus 로고
    • For recent reviews on palladium-catalyzed synthesis of indoles, see: a
    • For recent reviews on palladium-catalyzed synthesis of indoles, see: (a) Cacchi, S.; Fabrizi, G. Chem. Rev. 2005, 105, 2873.
    • (2005) Chem. Rev , vol.105 , pp. 2873
    • Cacchi, S.1    Fabrizi, G.2
  • 7
    • 0033599339 scopus 로고    scopus 로고
    • Selected references on the intermolecular α-arylation of ketones: (a) Kawatsura, M.; Hartwig, J. F. J. Am. Chem. Soc. 1999, 121, 1473.
    • Selected references on the intermolecular α-arylation of ketones: (a) Kawatsura, M.; Hartwig, J. F. J. Am. Chem. Soc. 1999, 121, 1473.
  • 10
    • 0034824575 scopus 로고    scopus 로고
    • Selected references on the intermolecular α-arylation of esters: (a) Moradi, W. A.; Buchwald, S. L. J. Am. Chem. Soc. 2001, 123, 7996.
    • Selected references on the intermolecular α-arylation of esters: (a) Moradi, W. A.; Buchwald, S. L. J. Am. Chem. Soc. 2001, 123, 7996.
  • 13
    • 4544230318 scopus 로고    scopus 로고
    • Selected references on the intermolecular α-arylation of amides: (a) de Filippis, A.; Gomez Pardo, D.; Cossy, J. Tetrahedron 2004, 60, 9757.
    • Selected references on the intermolecular α-arylation of amides: (a) de Filippis, A.; Gomez Pardo, D.; Cossy, J. Tetrahedron 2004, 60, 9757.
  • 15
    • 0037077528 scopus 로고    scopus 로고
    • Intermolecular α-arylation of nitriles; (a) Culkin, D. A.; Hartwig, J. F. J. Am. Chem. Soc. 2002, 124, 9330.
    • Intermolecular α-arylation of nitriles; (a) Culkin, D. A.; Hartwig, J. F. J. Am. Chem. Soc. 2002, 124, 9330.
  • 18
    • 0036134669 scopus 로고    scopus 로고
    • Intermolecular α-arylation of aldehydes; (a) Terao, Y.; Fukuoka, Y.; Satoh, T.; Miura, M.; Nomura, M. Tetrahedron Lett. 2002, 43, 101.
    • Intermolecular α-arylation of aldehydes; (a) Terao, Y.; Fukuoka, Y.; Satoh, T.; Miura, M.; Nomura, M. Tetrahedron Lett. 2002, 43, 101.
  • 20
    • 0037169136 scopus 로고    scopus 로고
    • Selected references on the intermolecular α-arylation of 1,3-dicarbonyl compounds: (a) Beare, N. A.; Hartwig, J. F. J. Org. Chem. 2002, 67, 541.
    • Selected references on the intermolecular α-arylation of 1,3-dicarbonyl compounds: (a) Beare, N. A.; Hartwig, J. F. J. Org. Chem. 2002, 67, 541.
  • 51
    • 1642416676 scopus 로고    scopus 로고
    • For the Pd-catalyzed coupling with β,γ-unsaturated nitronates, see
    • For the Pd-catalyzed coupling with β,γ-unsaturated nitronates, see: Solé, D.; Urbaneja, X.; Bonjoch, J. Tetrahedron Lett. 2004, 45, 3131.
    • (2004) Tetrahedron Lett , vol.45 , pp. 3131
    • Solé, D.1    Urbaneja, X.2    Bonjoch, J.3
  • 55
    • 0343852084 scopus 로고
    • Trost, B. M, Fleming, I, Eds, Pergamon: Oxford
    • (b) Gribble, G. W. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 8, p 612.
    • (1991) Comprehensive Organic Synthesis , vol.8 , pp. 612
    • Gribble, G.W.1
  • 60
    • 41849107133 scopus 로고    scopus 로고
    • The formation of products from hydrodehalogenation and dealkylation of the starting material has been reported; see ref 12a
    • The formation of products from hydrodehalogenation and dealkylation of the starting material has been reported; see ref 12a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.