Conformation of linear homo‐oligoprolines: VII. N‐Pivaloyl‐l‐prolyl‐d‐proline methyl ester in the solid state
International Journal of Peptide and Protein Research, ISSN: 1399-3011, Vol: 20, Issue: 4, Page: 312-319
1982
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Article Description
A conformational analysis of Piv‐l‐Pro‐d‐Pro‐OMe was performed in the solid state using i.r. absorption and X‐ray diffraction. The tertiary amide bond is in the trans conformation, whereas the tertiary peptide bond is in the cis conformation. The sequence of the, ø angles is F, F*. The preferred conformations of the pivaloylamino group, the pyrrolidine rings, and the ester moiety are also discussed. © 1982 Munksgaard, Copenhagen
Bibliographic Details
Wiley
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