Conformational Analysis of Peptides and Pseudopeptides Incorporating an endo-(2S,3R)-Norborn-5-ene Residue as a Turn Inducer
- 20 February 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (5), 1505-1513
- https://doi.org/10.1021/jo971766t
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Design of a novel secondary structure scaffolding device: Induction of a reverse turn in tetrapeptides by incorporating a β-amino acid and stereocontrolled free radical α-substitution reactions in peptide motifsTetrahedron Letters, 1997
- Construction and Design of β-SheetsAccounts of Chemical Research, 1997
- Stabilization of a type VI turn in a family of linear peptides in water solutionJournal of Molecular Biology, 1994
- β-turn topographyTetrahedron, 1993
- Cis/trans conformational equilibrium across the cysteine6-proline peptide bond of oxytocin, arginine vasopressin, and lysine vasopressinJournal of the American Chemical Society, 1992
- Conformation-directing effects of a single intramolecular amide-amide hydrogen bond: variable-temperature NMR and IR studies on a homologous diamide seriesJournal of the American Chemical Society, 1991
- The Anatomy and Taxonomy of Protein StructureAdvances in protein chemistry, 1981
- Empirical Predictions of Protein ConformationAnnual Review of Biochemistry, 1978
- Über Antamanid, XVII1) Synthese weiterer antitoxisch wirksamer und unwirksamer Antamanid-VariantenEuropean Journal of Organic Chemistry, 1974
- Some aspects of NMR techniques for the conformational analysis of peptidesPublished by Walter de Gruyter GmbH ,1973