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- W1998803892 abstract "A cyclic hexapeptide, cyclo(Pro-Sar-Sar)2, which consists of N-substituted amino acids only was synthesized, and its solution conformation was investigated by n.m.r. spectroscopy. Seven different C2-symmetric conformations were detected, which were distinguishable from each other on the n.m.r. time scale. This is due to the cis/trans isomerization of N-substituted peptide bonds. Allowed C2-symmetric conformations were computed on the basis of a hard-sphere model. Some conformations detected in n.m.r. spectra were not allowed in the calculation. This disagreement suggests that some asymmetric conformations with regard to the single bond rotation are averaged out due to a rapid rotation on the n.m.r. time scale. These points indicate that the molecule of cyclo (Pro-Sar-Sar)2 is very flexible" @default.
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- W1998803892 date "1981-06-01" @default.
- W1998803892 modified "2023-09-24" @default.
- W1998803892 title "Synthesis and conformation of cyclic hexapeptide cyclo(Pro-Sar-Sar)2" @default.
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- W1998803892 doi "https://doi.org/10.1016/0141-8130(81)90061-1" @default.
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