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Volumn 46, Issue 21, 2010, Pages 3711-3713

Secondary orbital interactions in the propagation steps of lipid peroxidation

Author keywords

[No Author keywords available]

Indexed keywords

RADICAL;

EID: 77952378167     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/c0cc00019a     Document Type: Article
Times cited : (14)

References (24)
  • 2
    • 67650729358 scopus 로고    scopus 로고
    • and literature cited For recent contributions, see:
    • E. Niki Free Radical Biol. Med. 2009 47 469 484
    • (2009) Free Radical Biol. Med. , vol.47 , pp. 469-484
    • Niki, E.1
  • 8
    • 77952351175 scopus 로고    scopus 로고
    • In a recent example, Porter and co-workers 3a have shown that even olefin geometry plays a significant role on the product distribution of polyunsaturated hydrocarbon autoxidation
    • In a recent example, Porter and co-workers 3a have shown that even olefin geometry plays a significant role on the product distribution of polyunsaturated hydrocarbon autoxidation.
  • 11
    • 0345491105 scopus 로고
    • The larger basis was used for calculations involving propene/allyl, while the slightly smaller basis was used for pentadiene/pentadienyl
    • C. Lee W. Yang R. G. Parr Phys. Rev. B 1988 37 785 789
    • (1988) Phys. Rev. B , vol.37 , pp. 785-789
    • Lee, C.1    Yang, W.2    Parr, R.G.3
  • 13
    • 0038626673 scopus 로고    scopus 로고
    • Gaussian, Inc., Carnegie, PA, This interaction suggests that these reactions could be described to proceed by proton-coupled electron transfer. See:
    • All calculations were performed with the Gaussian 03 suite of programs. Gaussian 03, Gaussian, Inc., Carnegie, PA, 2003
    • (2003) Gaussian 03
  • 14
    • 34249088888 scopus 로고    scopus 로고
    • for a similar example: benzyl + toluene The calculated enthalpies of activation are the same for propene with either the smaller or larger basis sets
    • E. R. Johnson G. A. DiLabio J. Am. Chem. Soc. 2007 129 6199 6203
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 6199-6203
    • Johnson, E.R.1    Dilabio, G.A.2
  • 24
    • 70349826510 scopus 로고    scopus 로고
    • -1 lower in enthalpy than the concerted TS structure, now properly supporting the conclusion the allylperoxyl rearrangement takes place in a step-wise fashion as shown in Scheme 2A. See ESI for more information
    • A. G. Davies J. Chem. Res. 2009 533 544
    • (2009) J. Chem. Res. , pp. 533-544
    • Davies, A.G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.