The main transition of amorphous polymers is analyzed with respect to a fine structure by means of new experimental dynamic shear, dielectric, and heat capacity data for the following polymers : poly(n-alkyl methacrylate)s with alkyl = methyl, ethyl, propyl, butyl, and hexyl, polystyrene, poly(vinyl acetate), a series of weakly vulcanized natural rubbers, a series of butyl rubbers with different carbon black content, polyisobutylene, and bromobutyl rubber. The components of the fine structure are assumed to be a proper glass transition at short times, followed by a confined flow zone, and, at large times, a hindering zone caused by entanglements at large times. Two lengths are assumed to correspond to the first and third components, respectively, the characteristic length to the proper glass transition and the entanglement spacing to the hindering zone. The confined flow will be described by a dispersion law (general scaling) across the main transition. The characteristic length of the glass transition for the poly(n-alkyl methacrylate)s-only of order 1 nm as determined by calorimetry-is confirmed by backscaling from the entanglement spacing by means of a Rouse dispersion law for shear. The fate of the Rouse modes below the alpha beta splitting of the glass transition is discussed for the other amorphous polymers. Finally, a speculative molecular picture of the different modes in the main transition is described. The new element is a low-viscosity longitudinal motion of individual chain parts in the confined flow zone. A simple rheological model for the confined flow is also presented.