A convenient and versatile synthesis of 6,5- and 7,5-fused bicyclic lactams as peptidomimetics
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Peptidomimetics—Tailored Enzyme Inhibitors
2. Peptidomimetics for Receptor Ligands?Discovery, Development, and Medical Perspectives
3. Peptidomimetic synthesis: Utilization of N-acyliminium ion cyclization chemistry in the generation of 7,6- and 7,5-fused bicyclic lactams
4. Pro-D-NMe-Amino Acid and D-Pro-NMe-Amino Acid: Simple, Efficient Reverse-Turn Constraints
5. Synthesis and analysis of Leu-enkephalin analogues containing reverse turn peptidomimetics
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1. Friedel–Crafts Chemistry. Part 43. A Convergent Construction of Some New Bridged Aza-Bicyclic Analogues of Azocine, Azonine, and Azecine via Friedel–Crafts Ring Closures;Australian Journal of Chemistry;2015
2. 2.17 Addition to N-Acyliminium Ions of Heteroatoms such as Oxygen, Nitrogen, Sulfur, and Selenium as Internal Nucleophiles;Comprehensive Organic Synthesis II;2014
3. Incorporation of labile trans-4,5-difluoromethanoproline into a peptide as a stable label for 19F NMR structure analysis;Journal of Fluorine Chemistry;2013-08
4. Expedient Synthesis of Highly Potent Antagonists of Inhibitor of Apoptosis Proteins (IAPs) with Unique Selectivity for ML-IAP;ACS Chemical Biology;2013-02-05
5. ChemInform Abstract: A Convenient and Versatile Synthesis of 6,5- and 7,5-Fused Bicyclic Lactams as Peptidomimetics.;ChemInform;2010-05-24
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