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Volumn 47, Issue 21, 2008, Pages 3958-3961

"Carbocation watching" in solvolysis reactions

Author keywords

Kinetics; Nucleophilic aliphatic substitution; Reactive intermediates; S N2C+ mechanism; Solvolysis

Indexed keywords

KINETICS; NUCLEOPHILIC ALIPHATIC SUBSTITUTION; REACTIVE INTERMEDIATES; S N2C+ MECHANISM; SOLVOLYSIS;

EID: 53549133987     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200800354     Document Type: Article
Times cited : (22)

References (31)
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    • Carbonium Ions, 1-5 (Eds.: G. A. Olah, P. v. R. Schleyer), Wiley-Interscience, New York, 1968-1976;
    • b) Carbonium Ions, Vol. 1-5 (Eds.: G. A. Olah, P. v. R. Schleyer), Wiley-Interscience, New York, 1968-1976;
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    • 0012094605 scopus 로고
    • Ed, X. Creary, JAI, Greenwich
    • e) Advances in Carbocation Chemistry, Vol. 1 (Ed.: X. Creary), JAI, Greenwich, 1989;
    • (1989) Advances in Carbocation Chemistry , vol.1
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    • 0012043005 scopus 로고
    • Ed, J. Coxon, JAI, Greenwich
    • f) Advances in Carbocation Chemistry, Vol. 2 (Ed.: J. Coxon), JAI, Greenwich, 1995.
    • (1995) Advances in Carbocation Chemistry , vol.2
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    • 0037011289 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 4493-4495.
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 4493-4495
  • 17
    • 53549125632 scopus 로고    scopus 로고
    • In the initial phase of the reaction, the conductivity is partially due to the presence of the benzhydrylium ions. Since the maximum of the benzhydryliums ions is only 3% of the initial concentration of benzhydryl acetate, we have neglected the fact that the specific conductivity of benzhydrylium ions differs from that of trialkylammonium ions
    • In the initial phase of the reaction, the conductivity is partially due to the presence of the benzhydrylium ions. Since the maximum of the benzhydryliums ions is only 3% of the initial concentration of benzhydryl acetate, we have neglected the fact that the specific conductivity of benzhydrylium ions differs from that of trialkylammonium ions.
  • 19
    • 53549101086 scopus 로고    scopus 로고
    • N2 reactions under these conditions can be excluded: N. Streidl, A. Antipova, H. Mayr, unpublished results.
    • N2 reactions under these conditions can be excluded: N. Streidl, A. Antipova, H. Mayr, unpublished results.
  • 21
    • 4644237749 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 2302-2305.
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 2302-2305
  • 23
    • 0004152553 scopus 로고    scopus 로고
    • Eds, G. K. S. Prakash, P. v. R. Schleyer, Wiley-Interscience, New York
    • Stable Carbocation Chemistry (Eds.: G. K. S. Prakash, P. v. R. Schleyer), Wiley-Interscience, New York, 1997.
    • (1997) Stable Carbocation Chemistry
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.