| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 69662 | Journal of Molecular Catalysis B: Enzymatic | 2015 | 6 Pages |
•A one-pot chemoenzymatic cascade is described for the formation of γ-butyrolactones.•This approach is based on a lipase-catalyzed perhydrolysis and a chemical oxidation.•Baeyer–Villiger reaction has been successfully applied to 3-substituted cyclobutanones.•Lactones have been achieved in excellent isolated yields under mild conditions.•Purification of the final products was possible after a simple extraction protocol.
A one-pot chemoenzymatic method has been described for the synthesis of γ-butyrolactones starting from the corresponding ketones through a Baeyer–Villiger reaction. The approach is based on a lipase-catalyzed perhydrolysis for the formation of peracetic acid, which is the responsible for the ketone oxidation. Optimization studies have been performed in the oxidation of cyclobutanone, finding Candida antarctica lipase type B, ethyl acetate and urea-hydrogen peroxide complex as the best system. The relative ratio of these reagents has also been analyzed in depth. This synthetic approach has been successfully extended to a family of 3-substituted cyclobutanones in high substrate concentration, yielding the corresponding lactones with excellent isolated yields and purities, under mild reaction conditions and after a simple extraction protocol.
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