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Volumn 26, Issue 13, 1996, Pages 2561-2568

On a safe and practical method for the preparation of β-keto phosphonates

Author keywords

[No Author keywords available]

Indexed keywords

PHOSPHONIC ACID DERIVATIVE;

EID: 0029977310     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919608004568     Document Type: Article
Times cited : (22)

References (53)
  • 41
    • 7844230745 scopus 로고
    • Walker, H.G. ; Hauser, C.R. J. Am. Chem. Soc. 1946, 68, 1386 and Reynolds. G.A. ; Hauser, C.R. Org. Synth. Coll. Vol. IV, 708. J. Wiley ed. New York, N. Y. 1963.
    • (1946) J. Am. Chem. Soc. , vol.68 , pp. 1386
    • Walker, H.G.1    Hauser, C.R.2
  • 42
    • 7844230745 scopus 로고
    • J. Wiley ed. New York, N. Y.
    • Walker, H.G. ; Hauser, C.R. J. Am. Chem. Soc. 1946, 68, 1386 and Reynolds. G.A. ; Hauser, C.R. Org. Synth. Coll. Vol. IV, 708. J. Wiley ed. New York, N. Y. 1963.
    • (1963) Org. Synth. Coll. Vol. IV , vol.4 , pp. 708
    • Reynolds, G.A.1    Hauser, C.R.2
  • 47
    • 37049117122 scopus 로고
    • (b) Addition of hexanoylchloride to the corresponding sodium enolate was reported to give the β-keto ester in 25 % yield. See Durrant, G. ; Sutherland, J.K. J. Chem. Soc., Perkin 1 1972, 2582.
    • (1972) J. Chem. Soc., Perkin 1 , pp. 2582
    • Durrant, G.1    Sutherland, J.K.2
  • 48
    • 0023724182 scopus 로고
    • (c) For acylation of lithium enolate see Natchev, I.A. Tetrahedron 1988, 44, 6455.
    • (1988) Tetrahedron , vol.44 , pp. 6455
    • Natchev, I.A.1
  • 51
    • 8944248239 scopus 로고    scopus 로고
    • note
    • 5, 80 % yield ; R′ = Ph, 75 % yield after distillation).
  • 52
    • 8944221608 scopus 로고    scopus 로고
    • note
    • 5, 85 % yield ; R′ = Ph, 75 % yield after distillation).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.