Abstract

Cyclo[( R)-Cysteinyl-( R)-Cysteine]; Conformation; Molecular Modelling; NMR; Peptide The conformation in solution of the conformationally constrained cyclic dipeptide N-BOC-[cyclo-(R)-cysteinyl-(R)-cysteine] t-butyl ester is investigated by NMR and molecular mechanics techniques. The compound is found to exist as two slowly interconverting conformations in chloroform, both of which have a cis amide bond.

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