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. 1999 Feb;181(3):757–763. doi: 10.1128/jb.181.3.757-763.1999

FIG. 7.

FIG. 7

Possible mechanisms of spontaneous isomerization of a hypothetical primary product [(Z)-4-(2-carboxylatophenyl)-2-oxo-3-butenoate] to (E)-4-(2-carboxylatophenyl)-2-oxo-3-butenoate (compound II) in D2O. Compounds III and V are hypothetical intermediates in the nonenzymatic conversion from (Z)-4-(2-carboxylatophenyl)-2-oxo-3-butenoate to (E)-4-(2-carboxylatophenyl)-2-oxo-3-butenoate.