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Volumn 126, Issue 31, 2004, Pages 9645-9660

Catalytic regioselectivity control in ring-opening cycloisomerization of methylene- or alkylidenecyclopropyl ketones

Author keywords

[No Author keywords available]

Indexed keywords

ATOMS; CARBOXYLIC ACIDS; CATALYSIS; CHEMICAL BONDS; HYDROGENATION; KETONES; METHANE; REACTION KINETICS;

EID: 3543138426     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0494860     Document Type: Article
Times cited : (151)

References (82)
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    • (b) Ohta, T.; Takaya, H. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Paquette, L. A., Eds.; Pergamon: Oxford, 1991; Vol. 5, p 1185.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 1185
    • Ohta, T.1    Takaya, H.2
  • 40
    • 0035819971 scopus 로고    scopus 로고
    • For some of the most recent results from this group, see: (a) Ma, S.; Wu, S. Chem. Commun. 2001, 441.
    • (2001) Chem. Commun. , pp. 441
    • Ma, S.1    Wu, S.2
  • 51
    • 3543149802 scopus 로고    scopus 로고
    • note
    • int = 0.1005), parameters 199. CCDC 228763 contains the supplementary crystallographic data.
  • 52
    • 0003738434 scopus 로고
    • Prestch, E., Clerc, T., Seibl, J., Simon, W. (Translator: Biemann, K.); Springer-Verlag: Berlin
    • Tables of Spectral Data for Structure Determination of Organic Compounds; Prestch, E., Clerc, T., Seibl, J., Simon, W. (Translator: Biemann, K.); Springer-Verlag: Berlin, 1983; p. H-215.
    • (1983) Tables of Spectral Data for Structure Determination of Organic Compounds
  • 53
    • 0346981239 scopus 로고
    • 1m-y were prepared according to the following reference with slight modification; i.e., the corresponding N,N-dimethyl amide was used instead of the lithium carboxylate: Thomas, E. W.; Szmuszkovicz, J. R. J. Org. Chem. 1990, 55, 6054.
    • (1990) J. Org. Chem. , vol.55 , pp. 6054
    • Thomas, E.W.1    Szmuszkovicz, J.R.2
  • 55
    • 3543064359 scopus 로고    scopus 로고
    • note
    • int = 0.0457), no observation [I > 2σ(I)] 3824, parameters 257. CCDC 190370 contains the supplementary crystallographic data.
  • 56
    • 3543114675 scopus 로고    scopus 로고
    • note
    • We thank the referees for the suggestion of this possibility.
  • 60
    • 3543102905 scopus 로고    scopus 로고
    • note
    • int = 0.0260), no observation [I > 2σ(I)] 3607, parameters 191. CCDC 224467 contains the supplementary crystallographic data.
  • 61
    • 3543149803 scopus 로고    scopus 로고
    • note
    • int = 0.0368), no observation [I > 2σ(I)] 3441, parameters 239. CCDC 224466 contains the supplementary crystallographic data.
  • 68
    • 0033517689 scopus 로고    scopus 로고
    • (d) Alper, P. B.; Meyers, C.; Lerchner, A.; Siegel, D. R.; Carreira, E. M. Angew. Chem., Int. Ed. 1999, 38, 3186. For an account of nucleophilic ring-opening of cyclopropanes, see: Danishefsky, S. Acc. Chem. Res. 1979, 12, 66. We thank the referees for the suggestion of this possibility.
    • (1999) Angew. Chem., Int. Ed. , vol.38 , pp. 3186
    • Alper, P.B.1    Meyers, C.2    Lerchner, A.3    Siegel, D.R.4    Carreira, E.M.5
  • 69
    • 0043104432 scopus 로고
    • (d) Alper, P. B.; Meyers, C.; Lerchner, A.; Siegel, D. R.; Carreira, E. M. Angew. Chem., Int. Ed. 1999, 38, 3186. For an account of nucleophilic ring-opening of cyclopropanes, see: Danishefsky, S. Acc. Chem. Res. 1979, 12, 66. We thank the referees for the suggestion of this possibility.
    • (1979) Acc. Chem. Res. , vol.12 , pp. 66
    • Danishefsky, S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.