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Volumn 51, Issue 5, 1999, Pages 1073-1078

Preparation of 1,4-dioxenes from α-diazo-β-ketoesters

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL DERIVATIVE; ALCOHOL DERIVATIVE; AZO COMPOUND; CATECHOL; DIOXANE DERIVATIVE; ESTER DERIVATIVE; ETHYLENE GLYCOL; KETOESTER; RHODIUM; UNCLASSIFIED DRUG;

EID: 0033133861     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-98-8317     Document Type: Article
Times cited : (7)

References (26)
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    • 0001449601 scopus 로고
    • The insertion of alcohols into diazocarbons has been studied extensively. (a) A. F. Noels, A. Demonceau, N. Petiniot, A. J. Hubert, and Ph. Teyssie, Tetrahedron, 1982, 38, 2733. (b) B. Ganem, N. Ikota, V. B. Muralidharan, W. S. Wade, S. D. Young, and Y. Yukimoto, J. Am. Chem. Soc., 1982, 104, 6787. (c) C.-Y. P. Teng and B. Ganem, J. Am. Chem. Soc., 1984, 106, 2463. (d) J. R. Marshall and J. Walker, J. Chem. Soc., 1952, 467. (e) C. J. Moody and R. J. Taylor, Tetrahedron Lett., 1987, 28, 5351.
    • (1982) Tetrahedron , vol.38 , pp. 2733
    • Noels, A.F.1    Demonceau, A.2    Petiniot, N.3    Hubert, A.J.4    Teyssie, P.5
  • 15
    • 0000359548 scopus 로고
    • The insertion of alcohols into diazocarbons has been studied extensively. (a) A. F. Noels, A. Demonceau, N. Petiniot, A. J. Hubert, and Ph. Teyssie, Tetrahedron, 1982, 38, 2733. (b) B. Ganem, N. Ikota, V. B. Muralidharan, W. S. Wade, S. D. Young, and Y. Yukimoto, J. Am. Chem. Soc., 1982, 104, 6787. (c) C.-Y. P. Teng and B. Ganem, J. Am. Chem. Soc., 1984, 106, 2463. (d) J. R. Marshall and J. Walker, J. Chem. Soc., 1952, 467. (e) C. J. Moody and R. J. Taylor, Tetrahedron Lett., 1987, 28, 5351.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 6787
    • Ganem, B.1    Ikota, N.2    Muralidharan, V.B.3    Wade, W.S.4    Young, S.D.5    Yukimoto, Y.6
  • 16
    • 0001392308 scopus 로고
    • The insertion of alcohols into diazocarbons has been studied extensively. (a) A. F. Noels, A. Demonceau, N. Petiniot, A. J. Hubert, and Ph. Teyssie, Tetrahedron, 1982, 38, 2733. (b) B. Ganem, N. Ikota, V. B. Muralidharan, W. S. Wade, S. D. Young, and Y. Yukimoto, J. Am. Chem. Soc., 1982, 104, 6787. (c) C.-Y. P. Teng and B. Ganem, J. Am. Chem. Soc., 1984, 106, 2463. (d) J. R. Marshall and J. Walker, J. Chem. Soc., 1952, 467. (e) C. J. Moody and R. J. Taylor, Tetrahedron Lett., 1987, 28, 5351.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 2463
    • Teng, C.-Y.P.1    Ganem, B.2
  • 17
    • 37049147575 scopus 로고
    • The insertion of alcohols into diazocarbons has been studied extensively. (a) A. F. Noels, A. Demonceau, N. Petiniot, A. J. Hubert, and Ph. Teyssie, Tetrahedron, 1982, 38, 2733. (b) B. Ganem, N. Ikota, V. B. Muralidharan, W. S. Wade, S. D. Young, and Y. Yukimoto, J. Am. Chem. Soc., 1982, 104, 6787. (c) C.-Y. P. Teng and B. Ganem, J. Am. Chem. Soc., 1984, 106, 2463. (d) J. R. Marshall and J. Walker, J. Chem. Soc., 1952, 467. (e) C. J. Moody and R. J. Taylor, Tetrahedron Lett., 1987, 28, 5351.
    • (1952) J. Chem. Soc. , pp. 467
    • Marshall, J.R.1    Walker, J.2
  • 18
    • 0001365827 scopus 로고
    • The insertion of alcohols into diazocarbons has been studied extensively. (a) A. F. Noels, A. Demonceau, N. Petiniot, A. J. Hubert, and Ph. Teyssie, Tetrahedron, 1982, 38, 2733. (b) B. Ganem, N. Ikota, V. B. Muralidharan, W. S. Wade, S. D. Young, and Y. Yukimoto, J. Am. Chem. Soc., 1982, 104, 6787. (e) C. J. Moody and R. J. Taylor, Tetrahedron Lett., 1987, 28, 5351. (d) J. R. Marshall and J. Walker, J. Chem. Soc., 1952, 467. (e) C. J. Moody and R. J. Taylor, Tetrahedron Lett., 1987, 28, 5351.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 5351
    • Moody, C.J.1    Taylor, R.J.2
  • 19
  • 20
    • 0028354039 scopus 로고
    • Reports on the extension of this reaction to diols have been limited. (a) M. A. McKervey and S. Kulkowit, J. Chem. Soc., Chem. Commun., 1981, 616. (b) D. Haigh, Tetrahedron, 1994, 50, 3177.
    • (1994) Tetrahedron , vol.50 , pp. 3177
    • Haigh, D.1
  • 21
    • 84969808662 scopus 로고
    • The β-keto esters were either commericially available or prepared by one of the following two methods. a) D. W. Brooks, L. D-L. Lu, and S. Masamune, Angew. Chem., Int. Ed. Eng., 1979, 18, 72. (b) D. Haigh, Tetrahedron, 1994, 50, 3177.
    • (1979) Angew. Chem., Int. Ed. Eng. , vol.18 , pp. 72
    • Brooks, D.W.1    Lu, L.D.-L.2    Masamune, S.3
  • 22
    • 0001743806 scopus 로고
    • Reports on the extension of this reaction to diols have been limited. (a) M. A. McKervey and S. Kulkowit, J. Chem. Soc., Chem. Commun., 1981, 616. b) C. R. Holmquist and E. J. Roskamp, J. Org. Chem., 1989, 54, 3258.
    • (1989) J. Org. Chem. , vol.54 , pp. 3258
    • Holmquist, C.R.1    Roskamp, E.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.