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Volumn 38, Issue 15, 1997, Pages 2763-2766

5-exo versus 6-endo intramolecular carbolithiation of N-allyl-N-(2-lithioallyl)amines

Author keywords

[No Author keywords available]

Indexed keywords

PYRROLIDINE DERIVATIVE;

EID: 0030953523     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00465-6     Document Type: Article
Times cited : (35)

References (29)
  • 1
    • 0001433726 scopus 로고
    • Coxon, J. M., Ed.; JAI Press: Greenwich, CT, Mechanisms of Importance in Synthesis
    • (a) Bailey, W. F.; Ovaska, T. V. In Advances in Detailed Reaction Mechanisms; Coxon, J. M., Ed.; JAI Press: Greenwich, CT, 1994; Vol. 3, Mechanisms of Importance in Synthesis, pp. 251-273,
    • (1994) Advances in Detailed Reaction Mechanisms , vol.3 , pp. 251-273
    • Bailey, W.F.1    Ovaska, T.V.2
  • 25
    • 0342599479 scopus 로고    scopus 로고
    • note
    • Alternatively, the 5-exo product could rearrange to the 6-endo via a cyclopropyl derivative. See ref. 5.
  • 27
    • 0026040962 scopus 로고
    • (b) Bailey, W. F.; Khanolkar, A. D. Tetrahedron 1991, 47, 7727-7738. Cyclization of 1,2-disubstituted alkenes is only possible with an activating group such as phenyl, trimethylsilyl, or cyclopropyl: Bailey, W.F.; Gavaskar, K. V. Tetrahedron 1994, 50, 5957-5970.
    • (1991) Tetrahedron , vol.47 , pp. 7727-7738
    • Bailey, W.F.1    Khanolkar, A.D.2
  • 28
    • 0028260787 scopus 로고
    • (b) Bailey, W. F.; Khanolkar, A. D. Tetrahedron 1991, 47, 7727-7738. Cyclization of 1,2-disubstituted alkenes is only possible with an activating group such as phenyl, trimethylsilyl, or cyclopropyl: Bailey, W.F.; Gavaskar, K. V. Tetrahedron 1994, 50, 5957-5970.
    • (1994) Tetrahedron , vol.50 , pp. 5957-5970
    • Bailey, W.F.1    Gavaskar, K.V.2
  • 29
    • 0342599478 scopus 로고    scopus 로고
    • note
    • 13C NMR data.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.