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Volumn 62, Issue 16, 1997, Pages 5550-5556

Radical Ion Probes. 7. Behavior of a "Hypersensitive" Probe for Single Electron Transfer in Reactions Not Involving Electron Transfer

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EID: 0001064451     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo970584w     Document Type: Article
Times cited : (5)

References (30)
  • 4
    • 0012713033 scopus 로고
    • RN1 reaction, see: Bunnett, J. F.; Creary, X. J. Org. Chem. 1974, 39, 3174.
    • (1986) J. Org. Chem. , vol.51 , pp. 606
    • Meijs, G.F.1
  • 13
    • 85086288287 scopus 로고    scopus 로고
    • note
    • - to the solution results in a depression in reaction rate (i.e., the common-ion effect). See ref 9.
  • 14
    • 1542756400 scopus 로고    scopus 로고
    • note
    • Compound 1 has a tendency to polymerize in MeOH and EtOH, and as a consequence, the mass balances were only 56 and 72%, respectively, in these two solvents.
  • 16
    • 33947441989 scopus 로고
    • Grunwald, E.; Winstein, S. J. Am. Chem. Soc. 1948, 70, 846. For a review, see: Bentley, T. W.; Llewellyn, G. In Progress in Physical Organic Chemistry, Vol. 17; Taft, R. W., Ed.; Wiley: New York, 1990; PP 121-158.
    • (1948) J. Am. Chem. Soc. , vol.70 , pp. 846
    • Grunwald, E.1    Winstein, S.2
  • 17
    • 0000121091 scopus 로고
    • Taft, R. W., Ed.; Wiley: New York
    • Grunwald, E.; Winstein, S. J. Am. Chem. Soc. 1948, 70, 846. For a review, see: Bentley, T. W.; Llewellyn, G. In Progress in Physical Organic Chemistry, Vol. 17; Taft, R. W., Ed.; Wiley: New York, 1990; PP 121-158.
    • (1990) Progress in Physical Organic Chemistry , vol.17 , pp. 121-158
    • Bentley, T.W.1    Llewellyn, G.2
  • 18
    • 85086288281 scopus 로고    scopus 로고
    • note
    • neo) values.
  • 19
    • 85086289642 scopus 로고    scopus 로고
    • note
    • - and either 1 or 2 by UV proved troublesome because the reactions were over in less than 5 min, and the results were unacceptably erratic.
  • 21
    • 1542651093 scopus 로고    scopus 로고
    • note
    • For both 1 and 8, the bulky tert-butyl groups at the ortho position are expected to severely impede coordination of a Lewis acid with the carbonyl oxygen. We suspect that most of the observed changes in chemical shift observed for 8 are more a function of changes in the dielectric constant of the medium, rather than any close association of solvent or counterion with the oxygen.
  • 23
    • 0002631330 scopus 로고
    • Boger, D. L.; Johnson, D. S. Angew. Chem., Int. Ed. Engl. 1996, 33, 1438. See also: Boger, D. L. Acc. Chem. Res. 1995, 28, 20.
    • (1995) Acc. Chem. Res. , vol.28 , pp. 20
    • Boger, D.L.1
  • 30
    • 1542651088 scopus 로고
    • Aldrich Chemical Company; Milwaukee, WI
    • Aldrich Handbook of Fine Chemicals; Aldrich Chemical Company; Milwaukee, WI, 1993; p 604.
    • (1993) Aldrich Handbook of Fine Chemicals , pp. 604


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.