Amado, PatríciaFrija, Luís M. T.Coelho, Jaime A. S.O’Neill, Paul M.Cristiano, Maria De Lurdes2021-09-282021-09-282021http://hdl.handle.net/10400.1/17165A novel protocol for the preparation of nonsymmetrical 1,2,4,5-tetraoxanes and 1,2,4-trioxanes, promoted by the heterogeneous silica sulfuric acid (SSA) catalyst, is reported. Different ketones react under mild conditions with gemdihydroperoxides or peroxysilyl alcohols/beta-hydroperoxy alcohols to generate the corresponding endoperoxides in good yields. Our mechanistic proposal, assisted by molecular orbital calculations, at the.B97XD/def2-TZVPP/PCM(DCM)// B3LYP/6-31G(d) level of theory, enhances the role of SSA in the cyclocondensation step. This novel procedure differs from previously reported methods by using readily available and inexpensive reagents, with recyclable properties, thereby establishing a valid alternative approach for the synthesis of new biologically active endoperoxides.engjournal article10.1021/acs.joc.1c012581520-6904