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Volumn 46, Issue 1, 2010, Pages 130-132

Synthesis of 3-hydroxyoxindoles by Pd-catalysed intramolecular nucleophilic addition of aryl halides to α-ketoamides

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYINDOLE DERIVATIVE; ALPHA KETOAMIDE; AMIDE; HALIDE; INDOLE DERIVATIVE; NUCLEOPHILE; PALLADIUM; UNCLASSIFIED DRUG;

EID: 72149115697     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b917958e     Document Type: Article
Times cited : (95)

References (27)
  • 22
    • 60749131408 scopus 로고    scopus 로고
    • 3-Hydroxyoxindoles can be obtained by addition of aryl Grignard reagents or aryl lithium reagents (both are prepared from aryl halides) to isatin:
    • Y.-X. Jia E. P. Kündig Angew. Chem., Int. Ed. 2009 48 1636 1639
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 1636-1639
    • Jia, Y.-X.1    Kündig, E.P.2
  • 24
    • 37049047014 scopus 로고
    • and ref. cit. Catalytic asymmetric synthesis of 3-hydroxyoxindole: Pd catalysed intramolecular arylation of amides ref. 8b; M-catalysed addition of aryl boronic acids to isatin
    • S. J. Angyal E. Bullock W. G. Hanger W. C. Howell A. W. Johnson J. Chem. Soc. 1957 1592 1602
    • (1957) J. Chem. Soc. , pp. 1592-1602
    • Angyal, S.J.1    Bullock, E.2    Hanger, W.G.3    Howell, W.C.4    Johnson, A.W.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.