Synthesis and backbone conformations of cyclic hexapeptides cyclo-(Xxx-Pro-D-Gln)2
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1983.tb03104.x/fullpdf
Reference10 articles.
1. Solvent and side-chain contributions to the two-cis ? all-trans equilibria of cyclic hexapeptides,cyclo(Xxx-Pro-D-Yyy)2
2. Conformations of (X-L-Pro-Y)2 cyclic hexapeptides. Preferred .beta.-turn conformers and implications for .beta. turns in proteins
3. The Use of Esters of N-Hydroxysuccinimide in Peptide Synthesis
4. Eine neue Amid‐Schutzgruppe
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3. Structure determination and by-product profile of the NK2 receptor antagonist nepadutant, a bicyclic glycopeptide;FEBS Letters;2001-03-01
4. De-tert-butylation of substituted arenes;Tetrahedron;1998-11
5. Nmr and computer-aided studies of the three interchanging stereoisomers of the cyclic hexapeptidecyclo[-Pro1-Gly2-Glu3(OBzl)-Pro4-Phe5-Leu6-]: Unexpected observation of acis isomer of a secondary amide peptide bond in the presence of twotrans proline peptide bonds;Biopolymers;1993-04
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