Once a molecule is asymmetric, its extension proceeds also in an asymmetrical sense. This concept completely eliminates the difference between natural and artificial synthesis. The advance of science has removed the last chemical hiding place for the once so highly esteemed vis vitalis.

Their specific effect on the glucosides might thus be explained by assuming that the intimate contact between the molecules necessary for the release of the chemical reaction is possible only with similar geometrical configurations. To give an illustration I will say that enzyme and glucoside must fit together like lock and key in order to be able to exercise a chemical action on each other. This concept has undoubtedly gained in probability and value for stereochemical research, after the phenomenon itself was transferred from the biological to the purely chemical field. It is an extension of the theory of asymmetry without being a direct consequence of it: for the conviction that the geometrical structure of the molecule even for optical isomers exercises such a great influence on the chemical affinities, in my opinion could only be gained by new actual observations.