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 motifs
- 5 May 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (18) , 3155-3158
- https://doi.org/10.1016/s0040-4039(97)00612-6
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Pseudo-Prolines as a Molecular Hinge: Reversible Induction ofcisAmide Bonds into Peptide BackbonesJournal of the American Chemical Society, 1997
- Cyclic RGD Peptides Containing β-Turn MimeticsJournal of the American Chemical Society, 1996
- Peptide flexibility and calculations of an ensemble of moleculesJournal of the American Chemical Society, 1994
- Peptidomimetics for Receptor Ligands—Discovery, Development, and Medical PerspectivesAngewandte Chemie International Edition in English, 1993
- CONSTRAINED PEPTIDES: MODELS OF BIOACTIVE PEPTIDES AND PROTEIN SUBSTRUCTURESAnnual Review of Biochemistry, 1992
- Potent and highly selective neurokinin antagonistsJournal of Medicinal Chemistry, 1990
- Conformational constraints: Nonpeptide β‐turn mimicsJournal of Molecular Recognition, 1990
- Design and synthesis of a protein .beta.-turn mimeticJournal of the American Chemical Society, 1990
- The design and synthesis of mimetics of peptide β-turnsJournal of Molecular Recognition, 1988
- Design of Peptides and ProteinsAdvances in Protein Chemistry, 1988