메뉴 건너뛰기




Volumn 37, Issue 19, 1996, Pages 3319-3322

Microbiological transformations. 31: Synthesis of enantiopure epoxides and vicinal diols using fungal epoxide hydrolase mediated hydrolysis

Author keywords

[No Author keywords available]

Indexed keywords

ALKANEDIOL DERIVATIVE; EPOXIDE; HYDROLASE;

EID: 0030007179     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00540-0     Document Type: Article
Times cited : (17)

References (18)
  • 13
    • 20644469267 scopus 로고
    • Usually, the E value is obtained by measuring the ee of the residual substrate (ees) at a certain conversion ratio. However, in the case of biotransformations conducted using whole-cell cultures, it is very difficult to determine the degree of conversion with good accuracy because of the heterogeneity of the medium. Therefore, the E values are often determined using both ees and eep measurements, but this implies that the regioselectivity of the oxirane ring opening is identical for both enantiomers of the substrate
    • Chen, C.S.; Fujimoto, Y.; Girdaukas, G.; Sih, C.J. J. Am. Chem. Soc., 1982, 104, 7294. Usually, the E value is obtained by measuring the ee of the residual substrate (ees) at a certain conversion ratio. However, in the case of biotransformations conducted using whole-cell cultures, it is very difficult to determine the degree of conversion with good accuracy because of the heterogeneity of the medium. Therefore, the E values are often determined using both ees and eep measurements, but this implies that the regioselectivity of the oxirane ring opening is identical for both enantiomers of the substrate.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 7294
    • Chen, C.S.1    Fujimoto, Y.2    Girdaukas, G.3    Sih, C.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.