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Volumn 5, Issue 2, 2001, Pages 112-119

Synthetic applications of epoxide hydrolases

Author keywords

[No Author keywords available]

Indexed keywords

ELIPRODIL; EPOXIDE; EPOXIDE HYDROLASE; IBUPROFEN; MEVALONOLACTONE; NIFENALOL;

EID: 0035313421     PISSN: 13675931     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1367-5931(00)00179-4     Document Type: Review
Times cited : (216)

References (56)
  • 1
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    • Enantioselective epoxide hydrolysis: Catalysis involving microbes, mammals and metals
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    • Finney, N.S.1
  • 8
    • 0001515492 scopus 로고
    • Microbiological transformations. 19. Asymmetric dihydroxylation of the remote double bond of geraniol: A unique stereochemical control allowing easy access to both enantiomers of geraniol-6,7-diol
    • (1991) J Org Chem , vol.56 , pp. 3814-3817
    • Zhang, X.M.1    Archelas, A.2    Furstoss, R.3
  • 21
    • 0032768820 scopus 로고    scopus 로고
    • Affinity purification and characterisation of a yeast epoxide hydrolase
    • (1999) Biotechnol Lett , vol.21 , pp. 511-517
    • Botes, A.L.1
  • 39
    • 0033578911 scopus 로고    scopus 로고
    • Stereo- and enantioselectivity of the soluble epoxide hydrolase-catalysed hydrolysis of (+-)-cis-dialkyl substituted oxiranes
    • (1999) Tetrahedron , vol.55 , pp. 11589-11594
    • Chiappe, C.1    Palese, C.D.2
  • 45
    • 0032486416 scopus 로고    scopus 로고
    • Microbiological transformations 42. A two-phase preparative scale process for an epoxide hydrolase catalysed resolution of para-bromo α-methyl-styrene oxide. Occurrence of a surprising enantioselectivity enhancement
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 1839-1842
    • Cleij, M.1    Archelas, A.2    Furstoss, R.3
  • 46
    • 0035924935 scopus 로고    scopus 로고
    • Microbiological transformations 45. A green chemistry preparative scale synthesis of enantiopure building blocks of Eliprodil: Elaboration of a high substrate concentration epoxide hydrolase-catalyzed hydrolytic kinetic resolution process
    • (2001) Tetrahedron , vol.57 , pp. 695-701
    • Manoj, K.M.1    Archelas, A.2    Baratti, J.3    Furstoss, R.4
  • 47
    • 4243398971 scopus 로고    scopus 로고
    • St Quentin Fallavier, France: Sigma-Aldrich Chimie
    • (2001) Fluka catalog
  • 49
    • 0033067080 scopus 로고    scopus 로고
    • Microbial transformations 43. Epoxide hydrolase as tools for the synthesis of enantiopure α-methylstyrene oxides: A new and efficient synthesis of (S)-Ibuprofen
    • (1999) J Org Chem , vol.64 , pp. 5029-5035
    • Cleij, M.1    Archelas, A.2    Furstoss, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.