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Volumn , Issue 8, 1997, Pages 699-700

Preparation of m-acylphenol derivatives by the reaction of tricarbonyl(cyclohexadienone)iron complex and higher order cuprates

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EID: 0031520957     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1997.699     Document Type: Article
Times cited : (8)

References (13)
  • 1
    • 0000405865 scopus 로고
    • The bimolecular aromatic friedel-crafts reaction
    • ed by B. M. Trost, Pergamon Press, Oxford
    • H. Heaney, "The Bimolecular Aromatic Friedel-Crafts Reaction," in "Comprehensive Organic Synthesis." ed by B. M. Trost, Pergamon Press, Oxford (1991), Vol. 2, p 733.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 733
    • Heaney, H.1
  • 2
    • 0000137274 scopus 로고
    • 6-(Anisole)tricarbonylchromium complex is reported to read with an anion of cyanohydrin acetal to afford meta-acylanisole. M. F. Semmelhack and G. Clark. J. Am. Chem. Soc., 99, 1675 (1977).
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 1675
    • Semmelhack, M.F.1    Clark, G.2
  • 5
    • 37049133973 scopus 로고    scopus 로고
    • A. J. Birch, B. M. R. Bandara, K. Chamberlain, B. Chauncy, P. Dahler, A. I. Day, I. D. Jenkins, L. F. Kelly, T. C. Khor, G. Kretschmer, A. J. Liepa, A. S, Narula, W. D. Raverty, E. Rizzardo, C. Sell, R. Stephenson, D. J. Thompson, and D. H. Williamson, Tetrahedron, 37, Supplement No. 1, 289 (1981), R. J. H. Cowles, B. F. G. Johnson, J. Lewis and A. W. Parkins, J. Chem. Soc., Dalton Trans., 1972, 1768
    • J. Chem. Soc., Dalton Trans. , vol.1972 , pp. 1768
    • Cowles, R.J.H.1    Johnson, B.F.G.2    Lewis, J.3    Parkins, A.W.4
  • 6
    • 0041012244 scopus 로고    scopus 로고
    • S. E. Thomas, J. Chem. Soc., Chem. Commun., 1987. 226; T. N. Danks. D. Rakshit, and S. E. Thomas. J. Chem. Soc., Perkin Trans. 1, 1988, 2091.
    • J. Chem. Soc., Chem. Commun. , vol.1987 , pp. 226
    • Thomas, S.E.1
  • 8
  • 11
    • 0041012245 scopus 로고    scopus 로고
    • note
    • 3) δ = 0.81 (1.5H, 1, J = 7.4 Hz), 0.83 (1.5H, 1, 7.5 Hz), 1.01 (1.5H, d, J = 7.0 Hz), 1.03 (1.5H, d, J = 7.0 Hz), 1.31-1.34 (1H, m), 1.60-1.67 (1H, m), 2.02 (3H, s), 2.00-2.12 (1H. m), 2.51-2.54 (2H, m), 2.67-2.69 (1H. m), 3.05-3.25 (1H, m), 5.14 (1H, dd, J = 5.4 and 3.5 Hz), 5.33 (1H, d, J = 3.5 Hz).
  • 12
    • 0039233723 scopus 로고    scopus 로고
    • note
    • 3) δ = 0.73 (1.5H, t, J =7.4 Hz), 0.75 (1.5H, t, J = 7.4 Hz), 0.83 (1.5H, d, J = 6.8 Hz), 0.92 (1.5H, d, J = 6.8 Hz), 1.16-1.23 (2H, m), 1.41-1.55 (1H. m), 2.00-2.06 (1H, m), 2.08 (3H, s), 2.27-3.32 (1H, m), 2.35-2.42 (1H, m), 2.62-2.67 (1H. m), 4.36-4.40 (1H, m), 5.22-5.25 (1H. m), 7.35-7.42 (15H. m).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.