메뉴 건너뛰기




Volumn 24, Issue 19, 2002, Pages 1623-1630

Resolution of 4-(1-hydroxy-2,2,2-trifluoroethyl)phenol and its derivatives by lipase-catalyzed enantioselective alcoholysis

Author keywords

Alcoholysis; Enantioselectivity; Lipase; Phenol; Trifluoromethyl group

Indexed keywords

PSEUDOMONAS; PSEUDOMONAS AERUGINOSA;

EID: 0036802610     PISSN: 01415492     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1020305715636     Document Type: Article
Times cited : (7)

References (14)
  • 3
    • 0041152088 scopus 로고    scopus 로고
    • Properties and synthetic applications of enzymes in organic solvents
    • Carrea G, Riva S (2000) Properties and synthetic applications of enzymes in organic solvents. Angew. Chem. Intern. Edn. 39: 2226-2254.
    • (2000) Angew. Chem. Intern. Edn. , vol.39 , pp. 2226-2254
    • Carrea, G.1    Riva, S.2
  • 4
    • 20644469267 scopus 로고
    • Quantitative analysis of biochemical kinetic resolutions of enantiomers
    • Chen CS, Fujimoto Y, Girdaukas G, Sih CJ (1982) Quantitative analysis of biochemical kinetic resolutions of enantiomers. J. Am. Chem. Soc. 104: 7294-7299.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 7294-7299
    • Chen, C.S.1    Fujimoto, Y.2    Girdaukas, G.3    Sih, C.J.4
  • 6
    • 0028246441 scopus 로고
    • Highly stereocontrolled access to trifluoromethylbenzylic alcohols possessing p-substituents by the bakers' yeast reduction
    • Fujisawa T, Sugimoto, T, Shimizu M (1994) Highly stereocontrolled access to trifluoromethylbenzylic alcohols possessing p-substituents by the bakers' yeast reduction. Tetrahedron: Asymmetry 5: 1095-1098.
    • (1994) Tetrahedron: Asymmetry , vol.5 , pp. 1095-1098
    • Fujisawa, T.1    Sugimoto, T.2    Shimizu, M.3
  • 7
    • 0034744199 scopus 로고    scopus 로고
    • Regioselective substitution of phenols with trifluoroacetaldehyde ethyl hemiacetal
    • Gong Y, Kato K, Kimoto H (2001) Regioselective substitution of phenols with trifluoroacetaldehyde ethyl hemiacetal. Bull. Chem. Soc. Jpn. 74: 377-383.
    • (2001) Bull. Chem. Soc. Jpn. , vol.74 , pp. 377-383
    • Gong, Y.1    Kato, K.2    Kimoto, H.3
  • 8
    • 0033637004 scopus 로고    scopus 로고
    • Convenient synthesis of optically active 2,2,2-trifluoro-1-phenylethylamine
    • Kato K, Gong Y, Saito T, Kimoto H (2000) Convenient synthesis of optically active 2,2,2-trifluoro-1-phenylethylamine. Enantiomer 5: 521-524.
    • (2000) Enantiomer , vol.5 , pp. 521-524
    • Kato, K.1    Gong, Y.2    Saito, T.3    Kimoto, H.4
  • 9
    • 0035185406 scopus 로고    scopus 로고
    • Regio- and enantioselective acetylation of 3,3,3-trifluoro-2-arylpropane-1,2-diols using Candida antarctica lipase
    • Kato K, Gong Y. Saito T, Yokogawa Y (2001) Regio- and enantioselective acetylation of 3,3,3-trifluoro-2-arylpropane-1,2-diols using Candida antarctica lipase. Biotechnol. Lett. 23: 1729-1734.
    • (2001) Biotechnol. Lett. , vol.23 , pp. 1729-1734
    • Kato, K.1    Gong, Y.2    Saito, T.3    Yokogawa, Y.4
  • 10
    • 0029962076 scopus 로고    scopus 로고
    • Optical resolution of 2,2,2-trifluoro-1-(9-phenanthryl)ethanol via enzymatic alcoholysis of its activated ester
    • Kato K, Katayama M, Fujii S, Fukaya H. Kimoto H (1996) Optical resolution of 2,2,2-trifluoro-1-(9-phenanthryl)ethanol via enzymatic alcoholysis of its activated ester. J. Ferment. Bioeng. 81: 206-211.
    • (1996) J. Ferment. Bioeng. , vol.81 , pp. 206-211
    • Kato, K.1    Katayama, M.2    Fujii, S.3    Fukaya, H.4    Kimoto, H.5
  • 12
  • 14
    • 0033532260 scopus 로고    scopus 로고
    • Synthesis of (S)-1-(4-hydroxyphenyl)alcohols by eugenol dehydrogenase from Pseudomonas fluorescens E118
    • Wieser M, Furukawa H, Morita H, Yoshida T, Nagasawa T (1999) Synthesis of (S)-1-(4-hydroxyphenyl)alcohols by eugenol dehydrogenase from Pseudomonas fluorescens E118. Tetrahedron: Asymmetry 10: 1627-1630.
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 1627-1630
    • Wieser, M.1    Furukawa, H.2    Morita, H.3    Yoshida, T.4    Nagasawa, T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.