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Volumn 53, Issue 43, 1997, Pages 14793-14806

Mono- vs. dialkylation of carbanions. Effects of absolute and relative acidity of the conjugate carbon acids in selectivity control

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; CARBONIC ACID DERIVATIVE;

EID: 0342437478     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)00989-7     Document Type: Article
Times cited : (20)

References (32)
  • 1
    • 0343242284 scopus 로고    scopus 로고
    • note
    • This is the eighth of a series of papers dealing with selectivity of carbanion reactions; for previous papers see ref. 2.
  • 19
    • 0343242269 scopus 로고
    • Advances in Chemistry Series 215, Harris J. M. McManus S. P., Eds., ACS, Washington DC
    • (d) Bordwell F. G., Cripe T. A., Hughes D. L. Nucleophilicity. Advances in Chemistry Series 215, Harris J. M. McManus S. P., Eds., ACS, Washington DC 1987, p. 137-154.
    • (1987) Nucleophilicity , pp. 137-154
    • Bordwell, F.G.1    Cripe, T.A.2    Hughes, D.L.3
  • 22
    • 0342372698 scopus 로고    scopus 로고
    • note
    • The notion of counter balancing substituent effects, in this case the effect of carbanion basicity with carbon acid acidity, is not unknown. The first, and probably best known, is the formation by Taft of ES parameters from compensating substituent effects on acid catalysed hydrolysis, cf. ref. 11. According to a referee, this should be referenced as a support for the validity of the present arguments


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.