Design, Synthesis and Evaluation of Poly-l-Proline Type-II Peptide Mimics Based on the 3-Azabicyclo[3.1.0]hexane System
Author:
Affiliation:
1. Department of Chemistry, University of Vermont, Burlington, Vermont 05405
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo981814p
Reference11 articles.
1. The importance of extended conformations and, in particular, the PII conformation for the molecular recognition of peptides
2. Delineation of an Active Fragment and Poly(l-proline) II Conformation for Candidacidal Activity of Bactenecin 5
3. Pseudo-A(1,3) Strain as a Key Conformational Control Element in the Design of Poly-l-proline Type II Peptide Mimics
4. Conformational stability of proline oligomers
5. 1,2,3-Trisubstituted cyclopropanes as conformationally restricted peptide isosteres: application to the design and synthesis of novel renin inhibitors
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