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Volumn 125, Issue 1, 2003, Pages 151-157

Kinetic and thermodynamic acidities of substituted 1-benzyl-1-methoxy-2-nitroethylenes. Strong reduction of the transition state imbalance compared to other nitroalkanes

Author keywords

[No Author keywords available]

Indexed keywords

ACIDITY; DATA REDUCTION; MORPHOLOGY; NITROGEN COMPOUNDS; REDUCTION; THERMODYNAMIC PROPERTIES;

EID: 0037425555     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0211398     Document Type: Article
Times cited : (28)

References (75)
  • 40
    • 0348033598 scopus 로고    scopus 로고
    • note
    • 1 = 1). For proton transfers, statistical factors are usually included; see below.
  • 44
    • 0348033597 scopus 로고    scopus 로고
    • note
    • For discussions relating to the origins of the imbalance, see, for example, refs 3, 12, 16, 18, 20, and 21.]
  • 47
    • 0347402724 scopus 로고    scopus 로고
    • note
    • 23
  • 51
    • 0346141928 scopus 로고    scopus 로고
    • note
    • +. However, all experiments were conducted in a pH range where these terms are negligible.
  • 52
    • 0346141929 scopus 로고    scopus 로고
    • note
    • See paragraph concerning Supporting Information at the end of this paper.
  • 53
    • 0348033595 scopus 로고    scopus 로고
    • note
    • 29
  • 57
    • 0347402723 scopus 로고    scopus 로고
    • note
    • 34 and the same may very well be the case with 2-Z.
  • 62
    • 0347402722 scopus 로고    scopus 로고
    • note
    • Footnote d in Table 4.
  • 63
    • 0346141927 scopus 로고    scopus 로고
    • note
    • 4b
  • 65
    • 0346772345 scopus 로고    scopus 로고
    • note
    • 22 may itself be taken as strong evidence in support of the traditional view.
  • 71
    • 0347402721 scopus 로고    scopus 로고
    • note
    • ‡ = 0).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.