Solid phase synthesis of constrained 13-membered peptide macrocycles employing Fukuyama–Mitsunobu alkylations-Reference-Cited by-同舟云学术

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Solid phase synthesis of constrained 13-membered peptide macrocycles employing Fukuyama–Mitsunobu alkylations

Published:2015-05 Issue:19 Volume:56 Page:2456-2459
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Wang Lei,Liu Wang-Qing,Saraux Noémie,Vidal Michel,Broussy Sylvain

Funder

University Paris Descartes

Centre National de la Recherche Scientifique

ANR

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference31 articles.

1. The exploration of macrocycles for drug discovery — an underexploited structural class

2. Macrocycles Are Great Cycles: Applications, Opportunities, and Challenges of Synthetic Macrocycles in Drug Discovery

3. Design, synthesis, and diversification of ribosomally derived peptide macrocycles

4. Inhibition of α-helix-mediated protein–protein interactions using designed molecules

5. Constraining Cyclic Peptides To Mimic Protein Structure Motifs

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1. Impact of Hydrogen‐Bond Surrogate Model on Helix Stabilization and Development of Protein‐Protein Interaction Inhibitors;ChemistrySelect;2023-03-09

2. Synthesis of Amines and Ammonium Salts;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2023

3. Therapeutic peptides: current applications and future directions;Signal Transduction and Targeted Therapy;2022-02-14

4. Trimodular Solution‐Phase Protocol for Rapid Large‐Scale Synthesis of Hydrogen Bond Surrogate‐Constrained α‐Helicomimics;European Journal of Organic Chemistry;2021-03-05

5. Fukuyama reduction, Fukuyama coupling and Fukuyama–Mitsunobu alkylation: recent developments and synthetic applications;Molecular Diversity;2021-02-11

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