Selenium-containing molecules represent a valuable class of compounds with a variety of applications in chemical and biological fields. Selenated reagents are used as intermediates to introduce functional groups (e.g., double bonds) onto different substrates or in the synthesis of various selenated derivatives. Among the variety of selenium-containing reagents, silyl selenides are frequently used to transfer a selenated moiety due to the smooth functionalization of the Se-Si bond, which allows for the generation of selenium nucleophilic species under mild conditions. While the use of the analogous sulfur nucleophiles, namely silyl sulfides, has been widely explored, a relatively limited number of reports on selenosilanes have been provided. This contribution will focus on the application of selenosilanes as nucleophiles in a variety of organic transformations, as well as under radical and redox conditions. The use of silyl selenides to prepare metal complexes and as selenium precursors of materials for atomic layer deposition will also be discussed.
