The pathway with the name 4-Hydroxyacetophenone
 has the following structure: 
Result: 
CC(=O)OC1=CC=C(C=C1)O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/57d978b5-f55f-462e-a9dc-c5908d165973, SMIRKS = [#6:2]-[#8:1]-[#6:6](-[#1,#6:3])=[O:7]>>[H][#8]-[#6:2].[#8-:1]-[#6:6](-[#1,#6:3])=[O:7]) C1=C(C=CC(=C1)O)O
CC(=O)[O-]
CC(=O)C1=CC=C(C=C1)O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/36eb9d8a-a8e3-488c-a9c3-f07fd82e4af7, SMIRKS = [#6:4]([H])([H])([H])-[#6:1](=[O:5])-[c:2]1[c:6]([H])[c:7]([H])[c:8](-[$([O]([H])),$([N]([H])([H])),$([#6;H3]),$(F),$(Cl),$(S([O-])(=O)=O),$([N+](-[O-])=O),$([H]),$(O-[#6;H3]):9])[c:10]([H])[c:11]([H])1>>[#6:4]([H])([H])([H])-[#6:1](=[O:5])-[#8]-[c:2]1[c:6]([H])[c:7]([H])[c:8](-[$([O]([H])),$([N]([H])([H])),$([#6;H3]),$(F),$(Cl),$(S([O-])(=O)=O),$([N+](-[O-])=O),$([H]),$(O-[#6;H3]):9])[c:10]([H])[c:11]([H])1) CC(=O)OC1=CC=C(C=C1)O

Description: One of the aerobic strategies used by microorganisms to degrade ketones is to perform the Baeyer-Villiger oxidation to form an ester, which can then be readily hydrolyzed. The metabolism of cyclic and aliphatic ketones, for example, the biodegradation of cyclohexanone ([http://www.ncbi.nlm.nih.gov/pubmed/1261|Donoghue et al., 1975]) and 2-tridecanone ([http://www.ncbi.nlm.nih.gov/pubmed/925012|Britton et al., 1977]), has been reported. In addition, the degradation of aryl ketones, such as 4-hydroxyacetophenone ([http://www.ncbi.nlm.nih.gov/pubmed/11073896|Tanner et al., 2000]), can also proceed by formation of an ester by the action of a Baeyer-Villiger type of monooxygenase.
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