The synthetic potential of thiosilanes and selenosilanes toward various electrophiles is described, focusing on the synthesis of a representative range of thiocarbonyl, selenocarbonyl, -functionalized compounds and acyl-seleno derivatives. Reactions of silyl chalcogenides with epoxides, episulfides and aziridines allowed the synthesis of -hydroxy, -mercapto and -amino thiols, as well as of -substituted selenides and diselenides. A peculiar behaviour was observed in the reaction with episulfides, leading to 7-membered trithia- and dithiaseleno-heterocycles. Furthermore, carbodesilylation of -heterosubstituted organosilanes provided a smooth access to benzothiophene and benzofuran-derivatives.
Silicon-assisted synthesis and functionalization of sulfurated and selenated compounds / Capperucci, Antonella; Tanini, Damiano. - In: PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS. - ISSN 1042-6507. - ELETTRONICO. - 190:(2015), pp. 1320-1338. [10.1080/10426507.2015.1024790]
Silicon-assisted synthesis and functionalization of sulfurated and selenated compounds
CAPPERUCCI, ANTONELLA;TANINI, DAMIANO
2015
Abstract
The synthetic potential of thiosilanes and selenosilanes toward various electrophiles is described, focusing on the synthesis of a representative range of thiocarbonyl, selenocarbonyl, -functionalized compounds and acyl-seleno derivatives. Reactions of silyl chalcogenides with epoxides, episulfides and aziridines allowed the synthesis of -hydroxy, -mercapto and -amino thiols, as well as of -substituted selenides and diselenides. A peculiar behaviour was observed in the reaction with episulfides, leading to 7-membered trithia- and dithiaseleno-heterocycles. Furthermore, carbodesilylation of -heterosubstituted organosilanes provided a smooth access to benzothiophene and benzofuran-derivatives.File | Dimensione | Formato | |
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