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Volumn 116, Issue 16, 2012, Pages 4713-4730

Role of perferryl-oxo oxidant in alkane hydroxylation catalyzed by cytochrome P450: A hybrid density functional study

Author keywords

[No Author keywords available]

Indexed keywords

ABSTRACTING; ATOMS; CATALYSIS; CHEMICAL BONDS; DENSITY FUNCTIONAL THEORY; HYDROGEN; IODINE; PARAFFINS; PROPANE;

EID: 84860274239     PISSN: 15206106     EISSN: 15205207     Source Type: Journal    
DOI: 10.1021/jp211184y     Document Type: Article
Times cited : (19)

References (126)
  • 78
    • 0009023810 scopus 로고
    • In; Smith, V. H. Jr. Scheafer, H. F. III; Morokuma, K. Eds; D. Reidel: Boston, MA
    • Yamaguchi, K.; Takahara, Y.; Fueno, T. In Applied Quantum Chemistry; Smith, V. H., Jr.; Scheafer, H. F., III; Morokuma, K., Eds; D. Reidel: Boston, MA, 1986; pp 155-184.
    • (1986) Applied Quantum Chemistry , pp. 155-184
    • Yamaguchi, K.1    Takahara, Y.2    Fueno, T.3
  • 86
    • 84906388838 scopus 로고    scopus 로고
    • There can also be another potential route for generating the ferryl-hydroxo species without the involvement of the perferryl-oxo oxidant. This is the direct electron transfer from the substrate to the heme with concomitant proton transfer. This mechanism can be operative if the substrate is an excellent electron donor.(40b)
    • There can also be another potential route for generating the ferryl-hydroxo species without the involvement of the perferryl-oxo oxidant. This is the direct electron transfer from the substrate to the heme with concomitant proton transfer. This mechanism can be operative if the substrate is an excellent electron donor.(40b)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.