The same conformation in the crystal and in chloroform (NMR data) is displayed by the biphenyl-containing cyclopeptide 1, the biphenyl units of which have S,S configuration. It can be separated chromatographically from the atropisomers, (R,S) and (R,R), also formed in the synthesis. The conformation of 1 is stabilized by two hydrogen bonds between the short peptide chains.
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Brandmeier et al. (1989) studied this question.
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