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Volumn 99, Issue 9, 1977, Pages 3080-3087

Lithiation of Cyclopropyl and 2-Methylcyclopropyl Phenyl Sulfides. Addition to Carbonyl Partners

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EID: 0000666117     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00451a039     Document Type: Article
Times cited : (87)

References (58)
  • 1
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    • For some approaches other than cyclobutyl spiroannelatiori see V. V. Kane, Synth. Commun
    • For some approaches other than cyclobutyl spiroannelatiori see V. V. Kane, Synth. Commun., 6, 237 (1976);
    • (1976) , vol.6 , pp. 237
  • 10
    • 0001023266 scopus 로고
    • E. J. Corey and J. I. Shulman, J. Am. Chem. Soc., 92, 5522 (1970). For a review with further references, see A. P. Krapcho, Synthesis, 383 (1974).
    • (1970) J. Am. Chem. Soc. , vol.92 , pp. 5522
    • Corey, E.J.1    Shulman, J.I.2
  • 12
    • 0013583537 scopus 로고
    • J. Am. Chem. Soc., 95, 2038 (1973);
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 2038
  • 13
    • 33947085593 scopus 로고
    • J. Am. Chem. Soc., 95, 5321 (1973);
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 5321
  • 19
    • 0001472070 scopus 로고
    • For a few pertinent studies see M. C. Caserio, W. A. Graham, and J. D. Roberts
    • For a few pertinent studies see M. C. Caserio, W. A. Graham, and J. D. Roberts, Tetrahedron, 11, 171 (1960);
    • (1960) Tetrahedron , vol.11 , pp. 171
  • 34
    • 85022264414 scopus 로고    scopus 로고
    • unpublished observations.
    • B. M. Trost and W. C. Vladuchick, unpublished observations.
    • Trost, B.M.1
  • 37
    • 0007626426 scopus 로고
    • W. E. Truce, K. R. Hollister, L. B. Lindy, and J. E. Parr, J. Org. Chem., 33, 43 (1968). For a carbene approach to substituted derivatives see G. Boche and D. R. Schneider, Tetrahedron Lett., 4247 (1975).
    • (1968) J. Org. Chem. , vol.33 , pp. 43
    • Truce, W.E.1    Hollister, K.R.2    Lindy, L.B.3    Parr, J.E.4
  • 39
    • 2642700417 scopus 로고
    • Ring opening of cyclopropyl anions stabilized by electron withdrawing groups are known: see
    • Ring opening of cyclopropyl anions stabilized by electron withdrawing groups are known: see G. Boche, D. Martens, and H. V. Wagner, J. Am. Chem. Soc., 98, 2668 (1976);
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 2668
    • Boche, G.1    Martens, D.2    Wagner, H.V.3
  • 43
    • 85022296754 scopus 로고
    • in “Organic Sulfur Chemistry, Structure
    • C. J. M. Stirling, Ed. Butterworths, London
    • B. M. Trost in “Organic Sulfur Chemistry, Structure, Mechanism, and Synthesis”, C. J. M. Stirling, Ed., Butterworths, London, 1975, pp 237263.
    • (1975) , pp. 237263
    • Trost, B.M.1
  • 57
    • 77956681289 scopus 로고
    • For reviews, see ref 18 and Acc. Chem. Res., 7, 85 (1974).
    • For reviews, see ref 18 and B. M. Trost, Fortschr. Chem. Forsch., 41, 1 (1973); Acc. Chem. Res., 7, 85 (1974).
    • (1973) Fortschr. Chem. Forsch. , vol.41 , pp. 1
    • Trost, B.M.1


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