An account of the most commonly used reagents for the introduction of
the benzeneselenenyl (phenyl seleno) group is given. The review focuse
s on the various methods of its introduction as auxiliary, modifying o
r protective entity, and its subsequent removal, thereby often promoti
ng other reactions as cyclizations or double bond formation. Less emph
asis is laid on reactions of the phenylselenenylated intermediates wit
h the PhSe-group left intact utilizing its stabilizing properties on c
harged intermediates, on reagents with a modified phenyl group, e.g. c
hiral derivatives, or on reactions not involving intermediate C-Se-bon
d formation.