Recent Advances in the Synthesis of 5-Substituted 1 H-Tetrazoles: A Complete Survey (2013-2018)

70Citations
Citations of this article
70Readers
Mendeley users who have this article in their library.

Abstract

Tetrazoles are synthetic organic heterocyclic compounds comprising of high nitrogen content among stable heterocycles. Tetrazoles, chiefly 5-substituted 1 H-tetrazoles have been used as a bioisosteric replacement for carboxylic acids in medicinal chemistry. Various clinical drugs, including losartan, cefazolin, and alfentanil, contain the tetrazole moiety. There have been significant developments in the synthesis of 5-substituted 1 H-tetrazoles. Researchers are still working to develop more efficient and ecofriendly methods for their synthesis. In this review, we provide a comprehensive discussion of the recent advancements in the field of synthesis of 5-substituted 1 H-tetrazoles. 1 Introduction 2 The Role of 5-Substituted 1 H-Tetrazoles in Medicinal Chemistry 3 Synthesis of 5-Substituted 1 H-Tetrazoles 3.1 Microwave-Assisted Synthesis 3.2 Heterogeneous Catalysts 3.3 Nanoparticles as Heterogeneous Catalysts 3.4 Miscellaneous Methods 4 Sartans: A Class of Tetrazole-Based Commercial Drugs 5 Conclusions.

Cite

CITATION STYLE

APA

Mittal, R., & Awasthi, S. K. (2019). Recent Advances in the Synthesis of 5-Substituted 1 H-Tetrazoles: A Complete Survey (2013-2018). Synthesis (Germany), 51(20), 3765–3783. https://doi.org/10.1055/s-0037-1611863

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free