Enzyme-Catalysed Synthesis and Absolute Configuration Assignments of cis-Dihydrodiol Metabolites from 1,4-Disubstituted Benzenes

A series of ten cis‐dihydrodiol metabolites has been obtained by bacterial biotransformation of the corresponding 1,4‐disubstituted benzene substrates using Pseudomonas putida UV4, a source of toluene dioxygenase (TDO). Their enantiomeric excess (ee) values have been established using chiral stationary phase HPLC and 1H NMR spectroscopy. Absolute configurations of the majority of cis‐dihydrodiols have been established using stereochemical correlation and X‐ray crystallography and the remainder have been tentatively assigned using NMR spectroscopic methods but finally confirmed by circular dichroism (CD) spectroscopy. These configurational assignments support and extend the validity of an empirical model, previously used to predict the preferred stereochemistry of TDO‐catalysed cis‐dihydroxylation of ten 1,4‐disubstituted benzene substrates, to more than twenty‐five examples. Biocatalytic syntheses and stereochemical assignments: cis‐dihydrodiol metabolites from ten 1,4‐disubstituted benzene substrates have been isolated, stereochemically assigned, and used to confirm the validity of a predictive model for toluene dioxygenase‐catalysed cis‐hydroxylation of arenes.