메뉴 건너뛰기




Volumn 125, Issue 12, 2003, Pages 3406-3407

Epoxidation of olefins by hydroperoxo-ferric cytochrome P450

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; ALKANE DERIVATIVE; ALKENE DERIVATIVE; CAMPHOR; CYTOCHROME P450; EPOXIDE; HYDROPEROXIDE; IRON DERIVATIVE; MUTANT PROTEIN; OXYGEN; SULFIDE; SULFOXIDE;

EID: 0242585454     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja029272n     Document Type: Article
Times cited : (143)

References (23)
  • 5
    • 0242548148 scopus 로고    scopus 로고
    • note
    • The systematic name of P450cam is Cypl01.
  • 18
    • 0242548146 scopus 로고    scopus 로고
    • note
    • Substrate 2 was synthesized via pyridinium dichromate oxidation of 5-norbornen-2-ol (Aldrich).
  • 20
    • 0242717237 scopus 로고    scopus 로고
    • note
    • When reactions were run in the presence of catalase and superoxide dismutase, no difference was seen in the amount of product formed.
  • 21
    • 0242548147 scopus 로고    scopus 로고
    • note
    • GC/MS for 5-methylenylcamphor was done using a Finnigan 4500 GC/MS system with a Restek RTX-5 capillary column (30 m × 0.25 mm) with camphor as internal standard. For 5-norbornen-2-one, product was quantified on a DB-17 column with cyclohexene oxide as internal standard.
  • 22
    • 0242632913 scopus 로고    scopus 로고
    • note
    • Reactivity with 5-methylenylcamphor was confirmed both as a function of time and of T252A concentration. Product formation went up linearly with time for a minute and then the rate of formation began to fall off. In the experiment monitoring product formation as a function of T252A concentration, the amount of product formed was proportional to T252A concentration over the range from 0.25 μM to 0.75 μM.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.