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Volumn 46, Issue 5, 2005, Pages 735-737

Novel and convenient synthesis of 4(1H)quinolones

Author keywords

Leimgruber Batcho; Pd catalysis; Quinolones

Indexed keywords

QUINOLONE DERIVATIVE;

EID: 11844271994     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.12.046     Document Type: Article
Times cited : (46)

References (19)
  • 1
    • 0026715856 scopus 로고
    • We will use this name throughout the text. In most published articles the tautomeric form 4-hydroxyquinoline is used. For discussion of the keto-enol tautomerism see, A. Cruz, J. Elguero, P. Goya, and A. Martínez Tetrahedron 48 1992 6135 6150 and references cited therein
    • (1992) Tetrahedron , vol.48 , pp. 6135-6150
    • Cruz, A.1    Elguero, J.2    Goya, P.3    Martínez, A.4
  • 17
    • 11844256729 scopus 로고    scopus 로고
    • note
    • A highly non-polar by-product was observed on TLC when the catalyst:substrate ratio was 1:1. This side product was not characterized
  • 19
    • 84985641208 scopus 로고
    • We were not able to separate the isomers and the ratio of 3-methoxy-2-nitroacetophenone:3-methoxy-4-nitro-acetophenone (56:44) was determined by NMR spectrometry. We highly recommend the method published by Fürstner et al. for the preparation of pure 3-methoxy-2-nitroacetophenone A. Fürstner, D.N. Jumbam, and G. Seidel Chem. Ber. 127 1994 1125 1130
    • (1994) Chem. Ber. , vol.127 , pp. 1125-1130
    • Fürstner, A.1    Jumbam, D.N.2    Seidel, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.