The most important progress made in the last ten years in the production of
new electrophilic selenium reagents as well as in their reactivity towards
unsaturated compounds are presented and discussed. Several new selenium-pr
omoted, ring-closure reactions are illustrated and the factors controlling
the selectivity of the cyclization process are discussed. One-pot selenenyl
ation-deselenenylation sequences, which occur using only catalytic amounts
of the organoselenium reagents, are presented. Finally, the efficient asymm
etric syntheses, which are carried out with the recently described chiral n
on-racemic electrophilic selenenylating agents, are also surveyed.