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Volumn 2, Issue 6, 2000, Pages 827-829

Aberrant SRN1 reaction of 4-aminophenol with α,p-dinitrocumene: EPR observation of intermediates

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EID: 0001211082     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol005573v     Document Type: Article
Times cited : (7)

References (26)
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    • ACS Monograph 178; The American Chemical Society: Washington, D.C.
    • RN1 Mechanism; ACS Monograph 178; The American Chemical Society: Washington, D.C., 1983.
    • (1983) RN1 Mechanism
    • Rossi, R.A.1    Rossi, R.H.2
  • 14
    • 0344887064 scopus 로고
    • as of phenol, 4-aminophenol, and aniline in DMSO are 18.0, 19.7, and 30.6, respectively
    • as of phenol, 4-aminophenol, and aniline in DMSO are 18.0, 19.7, and 30.6, respectively.
    • (1988) Acc. Chem. Res. , vol.21 , pp. 456-463
    • Bordwell, F.G.1
  • 16
    • 0040416994 scopus 로고
    • McKinney, T. M.; Geske, D. H. J. Am. Chem. Soc. 1967, 89, 2806-2813. Terabe S.; Konaka, R. J. Am. Chem. Soc. 1973, 95, 4976-4986.
    • (1967) J. Am. Chem. Soc. , vol.89 , pp. 2806-2813
    • McKinney, T.M.1    Geske, D.H.2
  • 17
    • 0009031067 scopus 로고
    • McKinney, T. M.; Geske, D. H. J. Am. Chem. Soc. 1967, 89, 2806- 2813. Terabe S.; Konaka, R. J. Am. Chem. Soc. 1973, 95, 4976-4986.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 4976-4986
    • Terabe, S.1    Konaka, R.2
  • 18
    • 0000259579 scopus 로고
    • Tamura, R.; Yamawaki, K.; Azuma, N. J. Org. Chem. 1991, 56, 5743-5745. Tamura, R.; Kohno, M.; Utsunomiya, S.; Yamawaki, K.; Azuma, N.; Matsumoto, A.; Ishii, Y. J. Org. Chem. 1993, 58, 3953-3959.
    • (1991) J. Org. Chem. , vol.56 , pp. 5743-5745
    • Tamura, R.1    Yamawaki, K.2    Azuma, N.3
  • 25
    • 0041329001 scopus 로고    scopus 로고
    • Treatment of 8 with acetic anhydride under these reaction conditions gave only O-acetylation products
    • Treatment of 8 with acetic anhydride under these reaction conditions gave only O-acetylation products.


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