Pseudo-Prolines (Psi Pro) consist of (4S)-oxazolidine- and (4R)-thiazo
lidine-carboxylic acids derived from amino acids Ser, Thr and Cys. The
y represent new branched proline analogues in which variation of the s
ubstituents (R-1, R-2, R-3) results in different physicochemical and c
onformational properties. We summarise here the relevant chemical and
structural aspects of such super-prolines intended to constrain and co
ntrol the peptide backbone in beta-turn motifs or to alter the imide c
is-trans ratio.