Rule bt0353
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mono-carbon-substituted Benzenoid -> 1-substituted-2,3-dihydroxy Benzenoid
mono-halo-substituted Benzenoid -> 1-halo-2,3-dihydroxy Benzenoid
mono-pseudohalo-substituted Benzenoid -> 1-pseudohalo-2,3-dihydroxy Benzenoid
| Aerobic Likelihood: | | Likely |
EAWAG-BBD Reaction(s):
Diphenyl ether -----> 2,3-Dihydroxydiphenyl ether (reacID# r1450)
2-[(3-Hydroxy(phenyl)methyl)phenyl]-propanoate -----> 2-{3-[(2,3-Dihydroxyphenyl)(hydroxy)methyl]phenyl}propanoate (reacID# r1645)
Comments:
This rule handles the 2,3-dioxygenation of mono-substituted aromatics (bt0369) and subsequent oxidation to form the catechol derivative (bt0255). The substituents are based on "Reactions of Toluene Dioxygenase" and Hudlicky T, Gonzalez D, Gibson DT (1999) Aldrichimica Acta 32(2): 35-62. The aromatic hydrocarbon dioxygenases produce an activated dioxygen species that is thought to be sufficiently reactive to potentially functionalize most, if not all, aromatic ring carbon atoms (Lipscomb and Hoffman, 2005).
Similarities:
bt0005: vic-unsubstituted Aromatic --> vic-Dihydroxyaromatic
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Page Author(s):
Michael Turnbull
February 25, 2010
This is the EAWAG-BBD biotransformation rule, ruleID# bt0353.
It was generated on December 3, 2024 11:55:50 AM CST.
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