Search

Because of the importance of polyfunctional amines, C-N bond formation is important in synthetic organic chemistry. Here we present a neutral amination reaction using azides as the nitrogen source and arylboronic acids with a rhodium(I) catalyst to afford alkyl-aryl and aryl-aryl secondary amines. Natural products and pharmaceutical derivatives were applied, and gram-scale reactions were performed, which demonstrated the utility. Mechanistic experiments and DFT calculations suggested that the reaction involves a metal-nitrene intermediate.

We developed a facile, efficient method for synthesizing highly substituted 2-aminopyridines from unstable vinyl carbodiimides generated in situ in a one-pot transformation. A series of novel highly substituted 3-functionalized 2-aminopyridines were produced in good yields. Reaction mechanism studies, which included control experiments and density-functional theory (DFT) calculations, demonstrated that Rh and potassium carbonate played key roles in the cyclization step., (© 2022 Wiley-VCH GmbH.)

We developed a facile, efficient method for synthesizing highly substituted 2‐aminopyridines from unstable vinyl carbodiimides generated in situ in a one‐pot transformation. A series of novel highly substituted 3‐functionalized 2‐aminopyridines were produced in good yields. Reaction mechanism studies, which included control experiments and density‐functional theory (DFT) calculations, demonstrated that Rh and potassium carbonate played key roles in the cyclization step. [ABSTRACT FROM AUTHOR]

Isocyanates are widely applied in the fields of materials science, drug discovery and chemical industry processes. Palladium-catalyzed carbonylation of azides with carbon monoxide (CO) is reported as a powerful method for simple and efficient access to isocyanates, which are important precursors for preparing structurally meaningful urea, carbamate and amidine derivatives. In this account, we provide an overview on the synthesis of isocyanates and their subsequent reactions to obtain diverse nucleophilic addition products. In addition, with particular emphasis on our mechanistic studies of the Pd-catalyzed carbonylation process, we outline the identification of the actual catalytic species, the possible intermediates and some key factors in the catalytic cycle. 1 Introduction 2 Palladium-Catalyzed Reaction of Azides with CO and Subsequent Nucleophilic Additions 3 Mechanistic Studies on the Palladium-Catalyzed Reaction of Azides with CO 3.1 Studies on the Actual Catalytic Species and the Key Intermediates in the Activation and Carbonylation of Acyl Azides 3.2 Study of the Sulfonylurea Product Self-Catalyzed Carbonylation of Sulfonyl Azides 3.3 Study of the Actual Catalytic Pattern of the Pd/C Catalyst 4 Conclusion [ABSTRACT FROM AUTHOR]