Oligomerization of N-aminodipeptides: to the synthesis of heterogeneous backbone with 1:1 α:α-N-amino aminoacid residue patterns-Reference-Cited by-同舟云学术

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Oligomerization of N-aminodipeptides: to the synthesis of heterogeneous backbone with 1:1 α:α-N-amino aminoacid residue patterns

Published:2008-11 Issue:47 Volume:64 Page:10741-10753
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Felten Anne-Sophie,Dautrey Sébastien,Bodiguel Jacques,Vanderesse Régis,Didierjean Claude,Arrault Axelle,Jamart-Grégoire Brigitte

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference30 articles.

1. Promotion of Sheet Formation in α-Peptide Strands by a β-Peptide Reverse Turn

2. The World ofβ- andγ-Peptides Comprised of Homologated Proteinogenic Amino Acids and Other Components

3. Pseudo-peptides in Drug Discovery;Guichard,2004

4. β-Peptides: From Structure to Function

5. Oligopeptide Foldamers: From Structure to Function

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1. Synthesis of N‐aminophalimides derived from α‐amino acids: Theoretical study to find them as HDAC8 inhibitors by docking simulations and in vitro assays;Chemical Biology & Drug Design;2023-08-28

2. 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

3. Synthesis of a new tripod BODIPY dye bearing N-tert-Butoxycarbonyl amine and its acetylation;Synthetic Communications;2022-08-17

4. Modelling biologically important NH⋯π interactions;Russian Chemical Reviews;2022

5. Peptide N-Amination Supports β-Sheet Conformations;Angewandte Chemie International Edition;2017-01-20

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