Recent Development in N-Auxilixary-Assisted Intramolecular Amination for Amine Substrates
Yingsheng Zhao, Chao Wang, Jian Han
Abstract
Yingsheng Zhao, Chao Wang, Jian Han
Abstract
Direct coupling of N–H with C–H has aroused great attention in the last decades; during which the directing-group-assisted intramolecular C–N bond formation via transition metal has been achieved significant progress. Herein, we highlight the recent development in the directing-group-assisted intramolecular amination for amine substrates to build the important N-containing heterocyclic compounds. 1 Introduction 2 Triflamide-Promoted Intramolecular Amination 3 Picolinamide-Assisted Intramolecular Amination 4 Palladium-Catalyzed Intramolecular Amination under Assistance of Oxalyl Amide 5 Conclusion
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Direct coupling of N–H with C–H has aroused great attention in the last decades; during which the directing-group-assisted intramolecular C–N bond formation via transition metal has been achieved significant progress. Herein, we highlight the recent development in the directing-group-assisted intramolecular amination for amine substrates to build the important N-containing heterocyclic compounds. 1 Introduction 2 Triflamide-Promoted Intramolecular Amination 3 Picolinamide-Assisted Intramolecular Amination 4 Palladium-Catalyzed Intramolecular Amination under Assistance of Oxalyl Amide 5 Conclusion
Key concepts: Intramolecular force, Amination, Chemistry, Amide, Amine gas treating, Palladium, Combinatorial chemistry, Reductive amination