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Literature summary for 3.3.2.10 extracted from

  • Monfort, N.; Archelas, A.; Furstoss, R.
    Enzymatic transformations. Part 55: Highly productive epoxide hydrolase catalyzed resolution of an azole antifungal key synthon (2004), Tetrahedron, 60, 601-605.
No PubMed abstract available

Organism

Organism UniProt Comment Textmining
Aspergillus niger
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Source Tissue

Source Tissue Comment Organism Textmining
commercial preparation
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Aspergillus niger
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(R)-1-chloro-2-(2,4-difluorophenyl)-2,3-epoxypropane + H2O in a racemic mixture only the (R)-enantiomeric epoxide is converted to the (R)-enantiomeric diol Aspergillus niger (R)-3-chloro-2-(2,4-difluoro-phenyl)-propane-1,2-diol
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