Gallocatechin or gallocatechol (synonyms) has two chiral centres at positions 2 and 3, and thus four diastereoisomers. This is the same as with catechin. Gallocatechin has one more hydroxyl group at the B ring than catechin.
(+)-Gallocatechin is (2R,3S)-2-(3,4,5-Trihydroxyphenyl)-3,5,7-chromanetriol
(-)-Gallocatechin is (2S,3R)-2-(3,4,5-Trihydroxyphenyl)-3,5,7-chromanetriol
(+)-Epigallocatechin is (2S,3S)-2-(3,4,5-Trihydroxyphenyl)-3,5,7-chromanetriol
(-)-Epigallocatechin is (2R,3R)-2-(3,4,5-Trihydroxyphenyl)-3,5,7-chromanetriol
The two Gallocatechins and the two epi Gallocatechins indicated by Andreas Josef Schwab must be enantiomers or mirror image molecules that cannot be separated via achiral chromatography. On the other hand the Gallocatechins must easily separate from epiGallocatechins even in achiral chromatographysince they are diastereoisomers.