Various chemoenzymatic routes to optically pure biologically active di
hydropyridines are reviewed. The review is focused on influence on the
biotransformation of the main in vivo enzymatic activity of the hydro
lase (lipase, esterase, protease), the microorganism source of the lip
ase and the substituents of the 1,4-dihydropyridine ring, as well as t
he physicochemical properties of the solvent and the nature of the nuc
leophile. The influence of these variables in the desymmetrisation of
prochiral diesters or in the resolution of racemic compounds is analyz
ed.