Solid phase synthesis of N-aminodipeptides in high optical purity
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. New Synthesis of 1,1-Substituted Hydrazines by Alkylation of N-Acyl- or N-alkyloxycarbonylaminophthalimide Using the Mitsunobu Protocol
2. A New Synthetic Route to Protected α-Hydrazinoesters in High Optical Purity Using the Mitsunobu Protocol
3. Original and efficient method for the preparation of N-aminoamide pseudodipeptides in high optical purity
4. Very efficient one-pot conversion of N-aminophthalimide derivatives into the corresponding N-amino-di-tert-butyl imidodicarbonates
5. A new versatile linker for the solid-phase synthesis of secondary amines
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1. A lysine-based 2:1-[α/aza]-pseudopeptide series used as additives in polymeric membranes for CO2 capture: synthesis, structural studies, and application;RSC Advances;2023
2. Synthesis and Structural Characterization of 2:1 [α/Aza]-oligomers;European Journal of Organic Chemistry;2014-10-21
3. The X-ray Structure of N-(Acetylamino)phthalimide, an Atypical Triacylhydrazine;Journal of Chemical Crystallography;2013-11-13
4. Development of pseudopeptides and peptidomimetics as eukaryote proteasome inhibitors;Comptes Rendus Chimie;2009-10
5. Original and efficient synthesis of 2:1-[α/aza]-oligomer precursors;Tetrahedron Letters;2009-07
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