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Volumn 63, Issue 26, 1998, Pages 9684-9689

A comparison of the reactivity and mutagenicity of N-(benzoyloxy)-N- (benzyloxy)benzamides

Author keywords

[No Author keywords available]

Indexed keywords

BENZAMIDE DERIVATIVE;

EID: 0032567448     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo980863z     Document Type: Article
Times cited : (36)

References (36)
  • 5
    • 20644448276 scopus 로고    scopus 로고
    • Ph.D. University of New England
    • Hammond, G. P. Ph.D. University of New England, 1997.
    • (1997)
    • Hammond, G.P.1
  • 18
    • 20644467548 scopus 로고    scopus 로고
    • note
    • -1. For a compilation see, ref 19, p 514.
  • 21
    • 20644438083 scopus 로고    scopus 로고
    • note
    • 2 = 0.94) and a ρ value for the heterolysis step in the region of +1.5.
  • 29
    • 20644460866 scopus 로고    scopus 로고
    • In press
    • The HERON reaction pathway has recently been supported by density functional calculations at the B3LYP/6-31G(D) level. Glover, S.; Mo, G.; Rauk, A. Tetrahedron. In press.
    • Tetrahedron
    • Glover, S.1    Mo, G.2    Rauk, A.3
  • 34
    • 20644449328 scopus 로고    scopus 로고
    • note
    • Mutagenicity appears to increase with increasing aromatic character, i.e., N-acetoxy-N-alkoxybenzamides 1 < N-acetoxy-N-benzyloxybenzamides 2 < N-benzoyloxy-N-benzyloxybenzamides 7. In addition, N-acetoxy-N-butoxy-2-naphthamide (5500 revertants) is more than 10 times more mutagenic than N-acetoxy-N-butoxy-2-benzamide (477 revertants) in TA100 at 1 μmol/plate.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.