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Volumn 63, Issue 20, 1998, Pages 7103-7106

Enantio- and regioselective baeyer-villiger oxidations of 2- and 3-substituted cyclopentanones using engineered bakers' yeast

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0001644454     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo980737v     Document Type: Article
Times cited : (71)

References (26)
  • 17
    • 85034170532 scopus 로고    scopus 로고
    • 13C NMR data were not consistent with a symmetrical molecule
    • 13C NMR data were not consistent with a symmetrical molecule.
  • 18
    • 0000281042 scopus 로고
    • While other models for the active site of cyclohexanone monooxygenase have been constructed independently, the close structural relationship between the cyclopentanones and the cyclohexanones used to construct this model make it especially convenient for the present purpose. Other cyclohexanone monooxygenase active site models: Taschner, M. J.; Peddada, L.; Cyr, P.; Chen, Q. Z.; Black, D. J. NATO ASI Ser., Ser. C 1992, 381, 347-360;
    • (1992) J. NATO ASI Ser., Ser. C , vol.381 , pp. 347-360
    • Taschner, M.J.1    Peddada, L.2    Cyr, P.3    Chen, Q.Z.4    Black, D.5
  • 26
    • 85034170226 scopus 로고    scopus 로고
    • The inclusion of cyclopentanone during this step was empirically found to increase the efficiency of the yeast cells during the subsequent Baeyer-Villiger oxidations.
    • The inclusion of cyclopentanone during this step was empirically found to increase the efficiency of the yeast cells during the subsequent Baeyer-Villiger oxidations.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.