High-resolution NMR of anisotropic samples is typically performed by spinning the sample around an axis at the magic angle of 54.7degrees with the static magnetic field. Geometric and engineering constraints often prevent spinning at this specific angle. Implementations of magic angle field rotation are extremely demanding due to power requirements or an inaccessible geometry. We present a methodology for taking the magic out of MAS while still obtaining both isotropic and anisotropic spectral information during sample spinning or field rotation at arbitrary angles. Using projected-MAS, we obtained resolved scaled isotropic chemical shifts in inhomogeneously broadened spinning samples. Published by Elsevier B.V.