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Volumn 34, Issue 11, 1995, Pages 1225-1227

Reactions of Carbocations with π Nucleophiles: Polar Mechanism and No Outer Sphere Electron Transfer

Author keywords

carbocations; electron transfer reactions; electrophilic additions; linear free energy relationships; reaction mechanisms

Indexed keywords


EID: 33747560030     PISSN: 05700833     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.199512251     Document Type: Article
Times cited : (47)

References (29)
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    • Mayr, H.1
  • 21
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    • ox values are obtained from the intersection values, see: E. Ahlberg, V. D. Parker,. The details will be published elsewhere
    • (1980) Acta Chem. Scand. B , vol.34 , pp. 91-96
  • 26
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    • ET will only be slightly smaller than the maximal values used for our calculations.
  • 27
    • 0000440429 scopus 로고
    • Single Electron Transfer as Rate-Determining Step in an Aliphatic Nucleophilic Substitution.
    • N2 mechanisms for the reactions of anionic nucleophiles with alkyl halides by comparing observed rate constants and those expected for the electron transfer process: (a)
    • (1986) Acta Chemica Scandinavica , vol.40 , pp. 470-485
    • Lund, T.1    Lund, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.