Reaction of N -alkyl azetidines with triphosgene
Author:
Funder
University of Versailles St-Quentin-en-Yvelines
CNRS
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference30 articles.
1. Synthesis and Profiling of a Diverse Collection of Azetidine-Based Scaffolds for the Development of CNS-Focused Lead-like Libraries
2. Discovery and Optimization of an Azetidine Chemical Series As a Free Fatty Acid Receptor 2 (FFA2) Antagonist: From Hit to Clinic
3. Pharmacological Characterization of AZD5069, a Slowly Reversible CXC Chemokine Receptor 2 Antagonist
4. Synthesis and preliminary biological evaluation of potent and selective 2-(3-alkoxy-1-azetidinyl) quinolines as novel PDE10A inhibitors with improved solubility
5. Fatty acid amide hydrolase inhibitors. Surprising selectivity of chiral azetidine ureas
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1. Synthesis of α-fluoro-γ-aminobutyric acid derivatives by nucleophilic ring-opening of azetidine-2-carboxylic acid-derived ammonium salts with fluoride;Tetrahedron;2023-08
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4. Diastereoselective ring cleavage of azetidines with cyanogen bromide;Tetrahedron Letters;2022-03
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