A new one-pot solvent-free synthesis of pyridinyl tosylates via diazotization of aminopyridines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Nickel-catalyzed coupling reaction of lithium organoborates and aryl mesylates possessing an electron withdrawing group
2. Room-Temperature Ni(0)-Catalyzed Cross-Coupling Reactions of Aryl Arenesulfonates with Arylboronic Acids
3. NiCl2(PCy3)2: A Simple and Efficient Catalyst Precursor for the Suzuki Cross-Coupling of Aryl Tosylates and Arylboronic Acids
4. Expanding Pd-Catalyzed C−N Bond-Forming Processes: The First Amidation of Aryl Sulfonates, Aqueous Amination, and Complementarity with Cu-Catalyzed Reactions
5. Ferrocenylmethylphosphines as ligands for room temperature Ni(0)-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl arenesulfonates and aryl chlorides
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2. A Novel and Simple Synthesis of Ethers of Hydroxypyridines with Hexafluoropropan-2-ol via Diazotization of Aminopyridines and Aminoquinolines Under Acid-Free Conditions;Chemistry of Heterocyclic Compounds;2022-12
3. Arenediazonium sulfonates: synthesis, comparison of structural and physicochemical properties;Bulletin of the Karaganda University. "Chemistry" series;2022-03-30
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