Synthesis of an azabicycloalkane amino acid scaffold as potential rigid dipeptide mimetic
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Design and synthesis of conformationally constrained amino acids as versatile scaffolds and peptide mimetics
2. Conformation of the tripeptide Cbz-Pro-Leu-Trp-OBzl(CF3)2deduced from two-dimensional1H-NMR and conformational energy calculations is related to its affinity for NK1-receptor
3. A flexible approach to the design of new potent substance P receptor ligands
4. Synthesis of Enantiopure .alpha.,.omega.-Diamino Dicarboxylates and Azabicycloalkane Amino Acids by Claisen Condensation of .alpha.-[N-(Phenylfluorenyl)amino] Dicarboxylates
5. Synthesis of 6,5-fused bicyclic lactams as potential dipeptide β-turn mimetics
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5. Bicyclic 5-6 Systems with One Bridgehead (Ring Junction) Nitrogen Atom: No Extra Heteroatom 0:0;Comprehensive Heterocyclic Chemistry III;2008
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