Controlled two-step nucleophilic hydroalkylations, hydroarylations as
well as hydrostannylations of fullerene-60 (1) and fullerene-70 (2) le
ad to defined organodihydrofullerenes Cr60HR and C70HR. NMR investigat
ions show that only one isomer of each organodihydrofullerene with C(s
) symmetry is formed. In all cases the addition takes place at a doubl
e bond separating two six-membered rings of the fullerene core. In thi
s way a variety of organodihydrofullerenes also carrying functional gr
oups have been synthesized.