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Volumn 62, Issue 12, 1997, Pages 3927-3930

Chemistry of Arylalkyl Radical Cations: Deprotonation vs Nucleophilic Attack

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0009517490     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo961502r     Document Type: Article
Times cited : (20)

References (45)
  • 18
    • 33845374344 scopus 로고
    • (b) Pross has suggested that nucleophilic attack of radical cations is a "forbidden" process. Similar constraints might apply to proton transfer. Pross, A. J. Am. Chem. Soc. 1986, 108, 3537.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 3537
    • Pross, A.1
  • 25
    • 1542800602 scopus 로고
    • Thesis, Georgia Institute of Technology
    • Isaac, J. M.S. Thesis, Georgia Institute of Technology, 1988.
    • (1988)
    • Isaac, J.M.S.1
  • 37
    • 85033150340 scopus 로고    scopus 로고
    • note
    • In separate experiments which are not described here, we have observed that 9,10-diethylanthracene undergoes oxidative substitution under identical reaction conditions at rates that are at least 100 times slower.
  • 38
    • 0004032955 scopus 로고
    • Kochi, J. K., Ed.; Wiley: New York
    • (a) Russell, G. A. In Free Radicals; Kochi, J. K., Ed.; Wiley: New York, 1973; Vol. I.
    • (1973) Free Radicals , vol.1
    • Russell, G.A.1
  • 45
    • 85033132605 scopus 로고    scopus 로고
    • The author has deposited atomic coordinates for l-(N-pyridiniumyl)aceanthrene with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, U.K.
    • The author has deposited atomic coordinates for l-(N-pyridiniumyl)aceanthrene with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, U.K.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.