SNAr azidation of phenolic functions utilizing diphenyl phosphorazidate
Author:
Funder
Japan Society for the Promotion of Science
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference36 articles.
1. Modern Nucleophilic Aromatic Substitution;Terrier,2013
2. High Pressure Organic Chemistry; XI.1A New Convenient Synthesis of Aromatic Amines from Activated Phenols
3. Microwave-Assisted Amination from Aryl Triflates without Base and Catalyst
4. Ionic Liquids/[bmim][N3] Mixtures: Promising Media for the Synthesis of Aryl Azides by SNAr
5. An SNAr Approach to Sterically Hindered ortho-Alkoxybenzaldehydes for the Synthesis of Olefin Metathesis Catalysts
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1. Azide Ionic Liquids for Safe, Green, and Highly‐Efficient Azidation Reactions to Produce Azide Polymers;Angewandte Chemie International Edition;2023-11-22
2. Azide Ionic Liquids for Safe, Green, and Highly‐Efficient Azidation Reactions to Produce Azide Polymers;Angewandte Chemie;2023-11-22
3. Practical synthesis of tetrazoles from amides and phosphorazidates in the presence of aromatic bases;Tetrahedron;2022-02
4. Cutting edge of diphenyl phosphorazidate (DPPA) as a synthetic reagent – A fifty-year odyssey;Organic Chemistry Frontiers;2022
5. Ideas and Developments in Organic Synthesis-Blessed with Serendipity;Journal of Synthetic Organic Chemistry, Japan;2021-12-01
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