## Abstract The crystal and molecular structures of two α‐aminoisobutyric acid (Aib)‐containing diketopiperazines, cyclo(Aib‐Aib) 1 and cyclo(Aib‐L‐Ile) **2**, are reported. Cyclo(Aib‐Aib) crystallizes in the space group P1 with __a__ = 5.649(3), __b__ = 5.865(2), __c__ = 8.363(1), α = 69.89(6), β
Conformation of peptides containing α-Aminoisobutyric acid the crystal structure of Boc-Gly-l-Ala-Aib-OMe
✍ Scribed by Bosch, Roland ;Jung, Günther ;Winter, Werner
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 396 KB
- Volume
- 1982
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Abstract
Boc‐Gly‐L‐Ala‐Aib‐OMe (1) crystallizes in the space group __P__2~1~2~1~2~1~ with a = 10.043(3), b = 11.590(5), c = 16.779(1) Å, and Z = 4 (R value for 1859 symmetry independent reflexions: 0.043). On the basis of a 4 → 1 intramolecular hydrogen bond, the tripeptide forms a β‐turn type III, although the Cα atom in the Aib residue is not directly involved in the β‐turn ring system. Inter‐molecular hydrogen bonds link the single molecules to helical structures along [100].
📜 SIMILAR VOLUMES
The decapeptides Boc-(Aib-L-Ala)s-OMe and Boc-(Aib-L-Val)s-OMe have been studied by 270-MHz lH-nmr in CDCl3 and (CD&SO solutions. Intramolecular hydrogen-bonded NH groups have been delineated using the temperature and solvent dependence of the NH chemical shifts and differential broadening of the NH
## Abstract The CD spectra of the peptides Boc‐X‐(Aib‐X)~__n__~‐OMe (__n__ = 1, 2, 3) and Boc‐(Aib‐X)~5~‐OMe, where X = L‐Ala or L‐Val have been examined in several solvents. The X = Ala and Val peptides behave similarly in all solvents, suggesting that the Aib residues dominate the folding prefere
## Abstract The structures of two dehydropentapeptides, Boc–Pro–ΔPhe–Val–ΔPhe–Ala–OMe (**I**) and Boc–Pro–ΔPhe–Gly–ΔPhe–Ala–OMe (**II**) (Boc: __t__‐butoxycarbonyl), have been determined by nuclear magnetic resonance (NMR), circular dichroism (CD), and X‐ray crystallographic studies. The peptide **
The peptide N-Boc-L-Gly-dehydro-Phe-NHCH, was synthesized by the combination of N-Boc-L-Gly-dehydro-Phe azlactone and pethylamine. Th? peptide crystalliqes in orthorhoybic space group P2,2121 with a = 5.679( 2) A, b = 16.423(9) A, c = 19.198(10) A, V = 1791(2) A3, 2 = 4, d m = 1.212(5) Mg m-,, dc =