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Volumn 3, Issue 18, 2001, Pages 2935-2938

Electrophilic cyclizations of vinylcyclopropanols to tethered aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; CYCLOPROPANE DERIVATIVE; VINYL DERIVATIVE;

EID: 0035817978     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol016490x     Document Type: Article
Times cited : (40)

References (45)
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    • On sabbatical leave from Sunmoon University, Korea
    • (a) On sabbatical leave from Sunmoon University, Korea.
  • 2
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    • GlaxoSmithKline Pharmaceutical, King of Prussia, PA, 19406-0939
    • (b) Present address: GlaxoSmithKline Pharmaceutical, King of Prussia, PA, 19406-0939.
  • 4
    • 0001373505 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford
    • (b) Hudlicky, T.; Reed, J. W. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 5, pp 899-970.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 899-970
    • Hudlicky, T.1    Reed, J.W.2
  • 5
    • 0000065841 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford
    • (c) Piers, E. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 5, pp 971-988.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 971-988
    • Piers, E.1
  • 6
    • 0000729612 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford
    • (d) Bronson, J. J.; Danheiser, R. L. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 5, pp 999-1035.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 999-1035
    • Bronson, J.J.1    Danheiser, R.L.2
  • 26
    • 33947085264 scopus 로고
    • An alternative preparation of 1-vinyl-1-cyclopropanols involves the condensation of diphenylsulfonium cyclopropylide with ketones and subsequent treatment of the resulting oxaspiropentanes with lithium diethylamide: (a) Trost, B. M.; Boddanowicz, M. J. J. Am. Chem. Soc. 1973, 95, 5311.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 5311
    • Trost, B.M.1    Boddanowicz, M.J.2
  • 32
    • 0042221753 scopus 로고    scopus 로고
    • note
    • d).
  • 33
    • 0043224075 scopus 로고    scopus 로고
    • The individual proton and carbon chemical shifts of 23 were secured by COSY and HETCOR spectra
    • (b) The individual proton and carbon chemical shifts of 23 were secured by COSY and HETCOR spectra.
  • 34
    • 0042722864 scopus 로고    scopus 로고
    • note
    • d).
  • 35
    • 0043224071 scopus 로고    scopus 로고
    • note
    • ax).
  • 36
    • 0042221752 scopus 로고    scopus 로고
    • note
    • ax′).
  • 38
    • 0001626504 scopus 로고
    • and references therein
    • (b) Overman, L. E. Acc. Chem. Res. 1992, 25, 352 and references therein.
    • (1992) Acc. Chem. Res. , vol.25 , pp. 352
    • Overman, L.E.1
  • 43
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    • (a) Maruoka, K.; Concepcion, A. B.; Yamamoto, H. Synthesis 1994, 1283; J. Org. Chem. 1994, 59, 4725.
    • (1994) J. Org. Chem. , vol.59 , pp. 4725
  • 45
    • 0344334078 scopus 로고    scopus 로고
    • An alternative strategy could involve ring expansion of a vinylcyclobutanol intermediate; compare: Kocovsky, P.; Dunn, V.; Gogoll, A.; Langer, V. J. Org. Chem. 1999, 64, 101.
    • (1999) J. Org. Chem. , vol.64 , pp. 101
    • Kocovsky, P.1    Dunn, V.2    Gogoll, A.3    Langer, V.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.