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Volumn 45, Issue 19, 2004, Pages 3793-3796

Preparation of 3-arylmethylindoles as selective COX-2 inhibitors

Author keywords

3 Arylmethylindole; 3 Benzylindole; COX 2 inhibitor; Palladium; Reductive indole alkylation; TMSOTf

Indexed keywords

BENZALDEHYDE DERIVATIVE; CYCLOOXYGENASE 2 INHIBITOR; INDOLE DERIVATIVE; KETONE; LEWIS ACID; METHYL GROUP; ORGANIC COMPOUND; PALLADIUM; SULFUR DERIVATIVE; ZINC;

EID: 1842850684     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.03.068     Document Type: Article
Times cited : (31)

References (16)
  • 2
    • 1842857880 scopus 로고    scopus 로고
    • Indole and its Derivatives, Science and Synthesis
    • Thomas E.J. Georg Thieme, Stuttgart. Category 2; Chapter 10.13.
    • Joule J.A. Indole and its Derivatives, Science and Synthesis. Thomas E.J. Houben-Weyl Methods of Molecular Transformations. Vol. 10:2000;Georg Thieme, Stuttgart. Category 2; Chapter 10.13.
    • (2000) Houben-Weyl Methods of Molecular Transformations , vol.10
    • Joule, J.A.1
  • 9
    • 1842857890 scopus 로고    scopus 로고
    • No attempts were made to couple aromatic ketones
    • (f) No attempts were made to couple aromatic ketones.
  • 10
    • 1842857893 scopus 로고    scopus 로고
    • PCT Int. Appl. CODEN: PIXXD2 WO 0329212 A1 20030410, 2003, 46 pp.
    • Broka, C. A.; Campbell, J. A. (F. Hoffmann-La Roche Ag, Switz). PCT Int. Appl. CODEN: PIXXD2 WO 0329212 A1 20030410, 2003, 46 pp.
    • Broka, C.A.1    Campbell, J.A.2
  • 11
    • 1842836086 scopus 로고    scopus 로고
    • note
    • These examples show the potential of this method for the syntheses of CNS-related targets.
  • 12
    • 1842857889 scopus 로고    scopus 로고
    • note
    • +).
  • 13
    • 1842857901 scopus 로고    scopus 로고
    • note
    • +).
  • 14
    • 1842857894 scopus 로고    scopus 로고
    • note
    • - 327.
  • 15
    • 43949172388 scopus 로고
    • For related addition-elimination reactions of a 2-formyl N-OMe indole as well as the methodology for preparation, see:
    • For related addition-elimination reactions of a 2-formyl N-OMe indole as well as the methodology for preparation, see: Yamada F., Fukui Y., Shinmyo D., Somei M. Heterocycles. 35(1):1993;99.
    • (1993) Heterocycles , vol.35 , Issue.1 , pp. 99
    • Yamada, F.1    Fukui, Y.2    Shinmyo, D.3    Somei, M.4
  • 16
    • 1842846884 scopus 로고    scopus 로고
    • note
    • 1H NMR.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.