Liquid crystalline alkane-3,4-dienoates (allenylacetates) have been sy
nthesized. Most compounds incorporate a heterocyclic 1,3,4-thiadiazole
ring or a pyrimidine ring as a constituent of the rigid core. These a
xial chiral allene derivatives were at first obtained as racemic mixtu
res. Some of them were also synthesized in enantiomerically enriched f
orm by enantioselective synthesis. The compounds were investigated by
polarizing microscopy and by differential scanning calorimetry. The th
ree-ring compounds exhibit broad regions of smectic C-phases. The opti
cally active three-ring compounds show broad S-c-phases with moderate
values of spontaneous polarization.