Three-dimensional phase correction was successfully tested on two real organic structures: Firstly, on phyllochlorine ester, C33N402H38, where intitial phasing was made on the basis of a n idealized, plane chlorine ring model, the orientation and position of which had been determined by the convolution molecule method (cf. also Fig. 10). Secondly, on the rubidium salt of the "sulfolipid" RbSCg010H17 1391 (initial phasing by the heavy-atom technique with R b and S). In both cases strong, spurious maxima were introduced into the initial Fourier syntheses on account of symmetry elements; in the course of the phase correction these maxima disappeared.