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Volumn 340, Issue 1, 1998, Pages 1-10

Sultones in organic synthesis

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0001805214     PISSN: 09411216     EISSN: None     Source Type: Journal    
DOI: 10.1002/prac.19983400102     Document Type: Review
Times cited : (35)

References (71)
  • 11
    • 0000105081 scopus 로고
    • G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann, eds., c, Thieme, Stuttgart
    • For reviews on intramolecular Diels-Alder reactions, see: (a) D. Craig, Houben-Weyl, Methods of Organic Chemistry, G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann, eds., Vol. E 21 c, Thieme, Stuttgart 1995, p. 2872;
    • (1995) Methods of Organic Chemistry , vol.E21 , pp. 2872
    • Craig, D.1    Houben-Weyl2
  • 12
    • 0000048482 scopus 로고
    • B. M. Trost, I. Fleming, L. A. Paquette, eds., Pergamon Press, Oxford
    • (b) W. R. Roush, Comprehensive Organic Synthesis, B. M. Trost, I. Fleming, L. A. Paquette, eds., Pergamon Press, Oxford 1991, vol. 5, p. 513;
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 513
    • Roush, W.R.1
  • 13
    • 0002251962 scopus 로고
    • D. P. Curran, ed., Jai Press, Greenwich (CT)
    • (c) W. R. Roush, Advances in Cycloaddition, D. P. Curran, ed., vol. 2, Jai Press, Greenwich (CT) 1990, p. 91;
    • (1990) Advances in Cycloaddition , vol.2 , pp. 91
    • Roush, W.R.1
  • 20
    • 0030772750 scopus 로고    scopus 로고
    • For a review on a related sequence involving intramolecular Diels-Alder reaction of silicon-tethered trienes and subsequent desilylation, see: L. Fensterbank, M. Malacria, S. McN. Sieburth, Synthesis 1997, 813
    • Synthesis , vol.1997 , pp. 813
    • Fensterbank, L.1    Malacria, M.2    Sieburth, S.McN.3
  • 41
    • 85034188956 scopus 로고    scopus 로고
    • unpublished
    • MeLi is superior to LDA for elimination of 12a to 23 (P. Metz, U. Meiners, unpublished)
    • Metz, P.1    Meiners, U.2
  • 42
    • 0003075009 scopus 로고    scopus 로고
    • For alternative direct additions of nucleophiles to 7-oxabicyclo[2.2.1]hept-5-ene derivatives followed by ring opening, see: (a) P. Chiu, M. Lautens, Top. Curr. Chem. 190 (1997) 1;
    • (1997) Top. Curr. Chem. , vol.190 , pp. 1
    • Chiu, P.1    Lautens, M.2
  • 68
    • 85034196364 scopus 로고    scopus 로고
    • unpublished
    • MeLi is superior to LDA/TMEDA for elimination of 12e to 42 (P. Metz, J. Stölting, unpublished)
    • Metz, P.1    Stölting, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.