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Volumn 47, Issue 22, 2008, Pages 4231-4233

Expanding the [1,2]-aryl migration to the synthesis of substituted indoles

Author keywords

Anilines; Indoles; Rearrangement; Regioselectivity; Synthetic methods

Indexed keywords

CHEMICAL REACTIONS; ORGANOMETALLICS;

EID: 47049109962     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200705804     Document Type: Article
Times cited : (44)

References (20)
  • 1
    • 34547095509 scopus 로고    scopus 로고
    • For recent reviews on indole alkaloids and references to the biological activity of compounds containing the indole substructure, see a T. Kawasaki, K. Higuchi, Nat. Prod. Rep. 2007, 24, 843, and references therein;
    • For recent reviews on indole alkaloids and references to the biological activity of compounds containing the indole substructure, see a) T. Kawasaki, K. Higuchi, Nat. Prod. Rep. 2007, 24, 843, and references therein;
  • 2
    • 0004230722 scopus 로고    scopus 로고
    • Ed, G. A. Cordell, Academic Press, San Diego
    • b) J. E. Saxton in The Alkaloids, Vol. 51 (Ed.: G. A. Cordell), Academic Press, San Diego, 1998;
    • (1998) The Alkaloids , vol.51
    • Saxton, J.E.1
  • 6
    • 33746864043 scopus 로고    scopus 로고
    • For recent reviews on indole synthesis, see a
    • For recent reviews on indole synthesis, see a) G. R. Humphrey, J. T. Kuethe, Chem. Rev. 2006, 106, 2875;
    • (2006) Chem. Rev , vol.106 , pp. 2875
    • Humphrey, G.R.1    Kuethe, J.T.2
  • 9
    • 0010653530 scopus 로고    scopus 로고
    • Ed, E. J. Thomas, Thieme, Stuttgart
    • d) J. A. Joule in Science of Synthesis, Vol. 10 (Ed.: E. J. Thomas), Thieme, Stuttgart, 2000, p. 361;
    • (2000) Science of Synthesis , vol.10 , pp. 361
    • Joule, J.A.1
  • 12
    • 0003979828 scopus 로고    scopus 로고
    • Academic Press, San Diego
    • g) R. J. Sundberg, Indoles, Academic Press, San Diego, 1996.
    • (1996) Indoles
    • Sundberg, R.J.1
  • 17
    • 37049095951 scopus 로고    scopus 로고
    • The chlorohydrin was isolated in high yield in the reaction of 2-chloroacetophenone with a Grignard reagent even after prolonged aging; see J. Barluenga, J. Florez, M. Yus, J. Chem. Soc. Perkin Trans. 1 1983, 3019.
    • The chlorohydrin was isolated in high yield in the reaction of 2-chloroacetophenone with a Grignard reagent even after prolonged aging; see J. Barluenga, J. Florez, M. Yus, J. Chem. Soc. Perkin Trans. 1 1983, 3019.
  • 18
    • 1842693391 scopus 로고    scopus 로고
    • The dilithium reagent generated from N-2-bromophenylpivaloylamide reacted with α-chloroketone to form the 3-substituted indole; see P. A. Wender, A. W. White, Tetrahedron 1983, 39, 3767.
    • The dilithium reagent generated from N-2-bromophenylpivaloylamide reacted with α-chloroketone to form the 3-substituted indole; see P. A. Wender, A. W. White, Tetrahedron 1983, 39, 3767.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.