Abstract
N-Acylbenzotriazoles are valuable synthons in organic synthesis. They are particularly used as acylating agents and an alternative to acyl chlorides. They have been widely explored for a diverse range of applications. This review summarizes methods for the preparation of N-acylbenzotriazole derivatives and their diverse applications, in particular demonstrating their ability to serve as alternative acylating agents in organic transformations such as N-, O-, C-, and S-acylating agents for the convenient synthesis of a wide range of biologically important organic compounds. We also emphasize the synthesis of diverse compounds using benzotriazole ring cleavage (BtRC) methodology, including its pharmacophore study and some notable utilities as valuable starting materials, ligands, and intermediates in the field of organic synthesis.
1 Introduction
2 Synthesis of N-Acylbenzotriazoles
3 Applications of N-Acylbenzotriazoles in Organic Synthesis
3.1 N-Acylation Using N-Acylbenzotriazoles
3.2 C-Acylation of Heterocycles Using N-Acylbenzotriazoles
3.3 Preparation of β-Keto Esters and β-Diketones by Acylative Deacetylation
3.4 N-Acylbenzotriazoles Used for the Preparation of Other Valuable Intermediates
3.5 Benzotriazole Ring Cleavage (BtRC) Reactions
4 N-Acylbenzotriazoles as Catalysts and Ligands
5 Pharmacological Applications of N-Acylbenzotriazoles
6 Conclusions and Future Outlook
Key words
N-acylbenzotriazole - acylation - denitrogenative ring cleavage - acylative deacetylation - benzotriazole ring cleavage reactions
