This article presents an overview of high resolution magic angle spinning (
HRMAS) NMR applied to solid phase synthesis. The different interactions exi
sting in such samples are described and analyzed with respect to their effe
ct on the linewidth of the sample. The critical element leading to the rela
tively narrow linewidth observed in such compounds using HRMAS is shown to
be the averaging of the magnetic susceptibility differences at the resin be
ad / solvent interface. The hardware required to record such spectra is des
cribed with an emphasis on probe technology. Applications of HRMAS to a tet
rapeptide, an organic molecule and a polymer are presented here.