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Volumn 53, Issue 13, 1997, Pages 4921-4934

Ketalised α- and β-lithiated α,β-unsaturated ketones: New masked acylvinyl anion equivalents

Author keywords

[No Author keywords available]

Indexed keywords

1,3 DIOXOLANE DERIVATIVE; CYCLOALKANONE; KETONE;

EID: 0030992439     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)00187-7     Document Type: Article
Times cited : (29)

References (51)
  • 1
    • 0000196714 scopus 로고
    • For general reviews, see: (a) Werstiuk, N. H. Tetrahedron 1983, 39, 205-268.
    • (1983) Tetrahedron , vol.39 , pp. 205-268
    • Werstiuk, N.H.1
  • 4
    • 0004111873 scopus 로고
    • Hase, T., Ed; J. Wiley & Sons: New York, ch. 5
    • (d) Werstiuk, N. H. In Umpoled Synthons; Hase, T., Ed; J. Wiley & Sons: New York, 1987; ch. 5.
    • (1987) Umpoled Synthons
    • Werstiuk, N.H.1
  • 6
    • 0000645105 scopus 로고
    • Trost, B. M.; Fleming, I; Heathcock, C. H., Eds.; Pergamon: Oxford
    • (f) Kuwajima, I.; Nakamura, E. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I; Heathcock, C. H., Eds.; Pergamon: Oxford, 1991; vol. II, pp. 441-473.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 441-473
    • Kuwajima, I.1    Nakamura, E.2
  • 22
    • 0026737653 scopus 로고
    • For the analogous radical ω-enolate equivalents, see: (a) Foubelo, F.; Lloret, F.; Yus, M. Tetrahedron 1992, 48, 9531-9536.
    • (1992) Tetrahedron , vol.48 , pp. 9531-9536
    • Foubelo, F.1    Lloret, F.2    Yus, M.3
  • 36
    • 0030496093 scopus 로고    scopus 로고
    • (b) For a recent review, see: Yus, M. Chem. Soc. Rev. 1996, 155-161.
    • (1996) Chem. Soc. Rev. , pp. 155-161
    • Yus, M.1
  • 37
    • 0030569283 scopus 로고    scopus 로고
    • For the last papers on these topics from our laboratory, see: (a) Alonso, E.; Ramón, D. J.; Yus, M. Tetrahedron 1996, 52, 14341-14348.
    • (1996) Tetrahedron , vol.52 , pp. 14341-14348
    • Alonso, E.1    Ramón, D.J.2    Yus, M.3
  • 44
    • 0343350789 scopus 로고
    • and references cited therein
    • 2-hybridised organolithium compounds. See, for instance: Barluenga, J.; Fernández, J. R.; Yus, M. J. Chem. Research (S) 1986, 273; (M) 1986, 2401-2415, and references cited therein.
    • (1986) J. Chem. Research (S) , pp. 2401-2415
  • 50
    • 84920296938 scopus 로고    scopus 로고
    • note
    • + signal.
  • 51
    • 84920296937 scopus 로고    scopus 로고
    • note
    • For compounds 3aa, 9b and 12a it was not possible to obtain the corresponding HRMS due to their instability.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.