The use of γ-turn mimetics to define peptide secondary structure
- 15 March 1993
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 49 (17), 3479-3488
- https://doi.org/10.1016/s0040-4020(01)90208-x
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Three novel mimics for the construction of sterically constrained protein turn modelsTetrahedron Letters, 1990
- Design and synthesis of a protein .beta.-turn mimeticJournal of the American Chemical Society, 1990
- Conformational restriction of peptidyl immunogens with covalent replacements for the hydrogen bondVaccine, 1988
- The design and synthesis of mimetics of peptide β-turnsJournal of Molecular Recognition, 1988
- Peptide conformations. Part 31. The conformation of cyclosporin a in the crystal and in solutionHelvetica Chimica Acta, 1985
- Synthesis of a bicyclic dipeptide with the shape of β-turn central partTetrahedron Letters, 1985
- Amide proton exchange rates in a cyclic dodecapeptide of defined conformation. pH and conformation dependenceBiochemistry, 1983
- A new approach to conformationally restricted peptide analogs: Rigid β-bends. 1. Enkephalin as an exampleBiochemical and Biophysical Research Communications, 1982
- The design and synthesis of nonpeptide compounds as mimics of a conformation of methionine-enkephalineCanadian Journal of Chemistry, 1982
- Protected lactam-bridged dipeptides for use as conformational constraints in peptidesThe Journal of Organic Chemistry, 1982