The peptide N-Boc-L-Pro-dehydro-Leu-OCH3 was synthesized by coupling dehydroleucine methyl ester with Boc-Pro-OH. It was crystallized from its solution in a methanol-water mixture at 4Β°C and the crystals belong to the orthorhfmbic space group P2,2,2, with a = 10.239( 1) A, b = 19.276(4) A, c = 20.31
Assessment of Conformation of the Tetrapeptides Boc(L-Pro)4-OBn, Boc-(L-Aze-L-Pro)2-Opcp and Boc-[(L-Pro)3-L-Aze]-Opcp
β Scribed by L. Zand; F.-H. Tsai; C. G. Overberger
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Weight
- 715 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0037-9646
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π SIMILAR VOLUMES
The peptide N-Boc-L-Pro-dehydro-Phe-L-Gly-OH was synthesized by the usual workup procedure and finally coupling the N-Boc-L-Pro-dehydro-Phe to glycine. The geptide crystallizes monoclinic space group P2: with a = 8.951( ) A, b = 5.677(6) A, c = 21.192(11) A, p = 96.97(4)', V = 1069(1) A3, Z = 2, d,
In order to elucidate the molecular mechanisms of alkali ions conduction of poly(D,L-proline), which shows the typical behavior of an ion channel across membranes, conformations of the tetrmeric derivative Boc(~-Pro-bPro),OCH, in solution, in the presence of the Na+ ion, were investigated by CD and
I n w siriiteg! for i l i c asyminctric synthesis of non-protcinogcnic clipcptidcs haxed on the bislactim ether nicthod is dcscrihcd. The nnn-prc,trinopeilic aniino acid which is part of the dipcpiidc. is Iwilt 1117 sicrensclcctiucly at the bislitctini ether si;tgc. Subscqucntl). ilmc hial;iclim cil
## SYNOPSIS T h e peptide Boc-Val-Val-Aib-Pro-Val-Val-Val-OMe has been synthesized t o investigate the effect of introduction of a strong 8-turn promoting guest segment into a n oligopeptide with a tendency t o form extended structures. 'H-nmr studies in solution using analysis of N H group solven