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Volumn 10, Issue 6, 2008, Pages 1067-1070

Anionic n-fries rearrangement of n-alkyl-2-iodo anilides induced by lodine-magnesium exchange: Application for synthesis of strained 1,2,3-trisubstituted indoies

Author keywords

[No Author keywords available]

Indexed keywords

ANILIDE; ANION; INDOLE DERIVATIVE; IODINE; MAGNESIUM;

EID: 45549101636     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol7029905     Document Type: Article
Times cited : (16)

References (33)
  • 1
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    • For a recent review of indole-containing natural products, see: a
    • For a recent review of indole-containing natural products, see: (a) Faulkner, D. J. Nat. Prod. Rep. 1999, 16, 155.
    • (1999) Nat. Prod. Rep , vol.16 , pp. 155
    • Faulkner, D.J.1
  • 2
    • 0034006916 scopus 로고    scopus 로고
    • For reviews on indole syntheses, see
    • (b) Lounasmaa, M.; Tolvanen, A. Nat. Prod. Rep. 2000, 17, 175. For reviews on indole syntheses, see:
    • (2000) Nat. Prod. Rep , vol.17 , pp. 175
    • Lounasmaa, M.1    Tolvanen, A.2
  • 3
    • 58149165756 scopus 로고    scopus 로고
    • Sundberg, R. J, Ed, Academic: London
    • (a) Sundberg, R. J., Ed. Indoles; Academic: London, 1996.
    • (1996) Indoles
  • 4
    • 84943388739 scopus 로고
    • Pyrroles and their Benzo Derivatives: Synthesis and Applications
    • Katritzky, A. R, Rees, C. W, Eds, Pergamon: Oxford
    • (b) Sundberg, R. J. Pyrroles and their Benzo Derivatives: Synthesis and Applications. Katritzky, A. R., Rees, C. W., Eds.; Comprehensive Heterocyclic Chemistry, Vol. 4; Pergamon: Oxford, 1984; pp 313.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.4 , pp. 313
    • Sundberg, R.J.1
  • 5
    • 40749104841 scopus 로고
    • For a recent review on Fischer indole synthesis, see
    • (c) For a recent review on Fischer indole synthesis, see: Hughes, D. L. Org. Prep. Proced. Int. 1993, 25, 607.
    • (1993) Org. Prep. Proced. Int , vol.25 , pp. 607
    • Hughes, D.L.1
  • 19
  • 27
    • 0025860919 scopus 로고    scopus 로고
    • Only two reports described migration of benzoyl and carbamoyl groups which are not within the scope of Fries rearrangement: (a) Horne, S, Rodrigo, R. Chem. Commun. 1991, 1046
    • Only two reports described migration of benzoyl and carbamoyl groups which are not within the scope of Fries rearrangement: (a) Horne, S.; Rodrigo, R. Chem. Commun. 1991, 1046.
  • 28
    • 58149170928 scopus 로고    scopus 로고
    • MacNeil, S.; Wilson, B. J.; Snieckus, V. Org. Lett. 2006, 8, 1133. For a recent paper on photochemically induced Fries rearrangement, see: Ferrini, S.; Ponticelli, F.; Taddei, M. Org. Lett. 2007, 9, 69.
    • (b) MacNeil, S.; Wilson, B. J.; Snieckus, V. Org. Lett. 2006, 8, 1133. For a recent paper on photochemically induced Fries rearrangement, see: Ferrini, S.; Ponticelli, F.; Taddei, M. Org. Lett. 2007, 9, 69.
  • 31
    • 58149160663 scopus 로고    scopus 로고
    • Reference 8b
    • (c) Reference 8b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.