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Volumn 125, Issue 46, 2003, Pages 13954-13955

An X- (X = I, Br)-Triggered Ring-Opening Coupling Reaction of Cyclopropenes with Organic Halides

Author keywords

[No Author keywords available]

Indexed keywords

3,3 BIS(METHOXYCARBONYL)CYCLOPROP 1 ENE; BROMINE; CYCLOPROPENE DERIVATIVE; HALIDE; PROPYLENE; UNCLASSIFIED DRUG;

EID: 0242415140     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja038131y     Document Type: Article
Times cited : (52)

References (26)
  • 1
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    • For very recent synthetic transformations of alkenyl halides, see: (a) Nordmann, G.; Buchwald, S. L. J. Am. Chem. Soc. 2003, 125, 4978.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 4978
    • Nordmann, G.1    Buchwald, S.L.2
  • 3
    • 0003995267 scopus 로고    scopus 로고
    • Negishi, E., Ed.; John Wiley & Sons: New York
    • Alkenyl halides are reactive under transition-metal catalysts; for reviews, see: (a) Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E., Ed.; John Wiley & Sons: New York, 2002; Vol. 1.
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , vol.1
  • 6
    • 0242562841 scopus 로고
    • Katrizky, A. R., Meth-Cohn, O., Rees, C. W., Eds.; Pergamon: Oxford
    • For reviews, see: (a) Urch, C. J. In Comprehensive Organic Functional Group Transformations; Katrizky, A. R., Meth-Cohn, O., Rees, C. W., Eds.; Pergamon: Oxford, 1995; Vol. 2, pp 606-619.
    • (1995) Comprehensive Organic Functional Group Transformations , vol.2 , pp. 606-619
    • Urch, C.J.1
  • 7
    • 0242395630 scopus 로고
    • Trost, B. M., Fleming, I., Schreiber, S. L., Eds; Pergamon: Oxford
    • (b) Kelly, S. E. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Schreiber, S. L., Eds; Pergamon: Oxford, 1991; Vol. 1, pp 807-808.
    • (1991) Comprehensive Organic Synthesis , vol.1 , pp. 807-808
    • Kelly, S.E.1
  • 10
    • 0141893944 scopus 로고    scopus 로고
    • Cyclopropenes: Transformations
    • Thieme: Stuttgart, Germany
    • (c) Baird, M. S. Cyclopropenes: Transformations. In Houben-Weyl; Thieme: Stuttgart, Germany, 1997; Vol. E17d/2, p 2781.
    • (1997) Houben-Weyl , vol.E17D , Issue.2 , pp. 2781
    • Baird, M.S.1
  • 18
    • 0000659278 scopus 로고    scopus 로고
    • For an exceptional example of ligand effect on regioselective allylzincation of 1-trimethylsilyl (Ge,Sn)-cyclopropenone acetals, see: Nakamura, M.; Inoue, T.; Sato, A.; Nakamura, E. Org. Lett. 2000, 2, 2193.
    • (2000) Org. Lett. , vol.2 , pp. 2193
    • Nakamura, M.1    Inoue, T.2    Sato, A.3    Nakamura, E.4
  • 20
    • 0242647406 scopus 로고    scopus 로고
    • note
    • 1H NMR analysis of the crude mixture.
  • 21
    • 0242395634 scopus 로고    scopus 로고
    • note
    • int = 0.0872), number of observations [I > 2σ(I)] 2416, parameters 259. Supplementary crystallographic data has been deposited at the Cambridge Crystallographic Data Center, CCDC 217324.
  • 25
    • 0000702671 scopus 로고
    • For reviews, see: (a) Heck, R. F. Org. React. 1982, 27, 345.
    • (1982) Org. React. , vol.27 , pp. 345
    • Heck, R.F.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.