Laccase-catalyzed synthesis of 2,3-ethylenedithio-1,4-quinones

•Laccase-catalyzed cross-coupling of 1,2-ethanedithiol with substituted hydroquinones.•Green, one-pot, enzymatic synthesis of 2,3-ethylenedithio-1,4-quinones.•Stability of in situ generated 1,4-quinone vital factor in product formation.•Eco-friendly laccases catalyze the reduction of O2 to H2O.

Laccases (benzenediol:oxygen oxidoreductase EC 1.10.3.2) belong to the family of multicopper oxidases. These environmentally friendly enzymes require O2 as their only co-substrate and produce H2O as their sole by-product. As a result, they have acquired increasing use in biotechnological applications, particularly in the field of organic synthesis. In the current study, laccases have been employed to successfully couple 1,2-ethanedithiol to various substituted hydroquinones to produce novel 2,3-ethylenedithio-1,4-quinones in good yields via an oxidation–addition–oxidation–addition–oxidation mechanism. The reactions proceeded in one-pot under mild conditions (room temperature, pH 5.0). This study further supports the use of laccases as green tools in organic chemistry. Furthermore, it provides evidence that laccase-catalyzed cross-coupling reactions involving small thiols are possible, in spite of research that suggests small thiols are potent inhibitors of laccases.

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