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Volumn 18, Issue 5, 2008, Pages 1555-1558

Characterization of the two major CYP450 metabolites of ozonide (1,2,4-trioxolane) OZ277

Author keywords

1,2,4 Trioxolane; Antimalarial; CYP450; Ozonide; Synthetic peroxide

Indexed keywords

ANTIMALARIAL AGENT; CARBON; CYTOCHROME P450; DRUG METABOLITE; METHANOL; OZ 277; OZ 381; OZ 397; OZONIDE(1,2,4 TRIOXOLANE); UNCLASSIFIED DRUG;

EID: 39849090620     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2008.01.087     Document Type: Article
Times cited : (37)

References (15)
  • 10
    • 0000263296 scopus 로고    scopus 로고
    • (a) Although the mechanism of the Griesbaum coozonolysis is not completely understood, the facial selectivity in reactions of the putative enantiomeric carbonyl oxide intermediates parallels the facial selectivity in reactions of 5-substituted 2-adamantyl derivatives. This requires consideration of both electrostatic and hyperconjugative effects, as, for example, discussed and debated in the following reviews: W. Adcock N.A. Trout Chem. Rev. 99 1999 1415
    • (1999) Chem. Rev. , vol.99 , pp. 1415
    • Adcock, W.1    Trout, N.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.