Issue 62, 2021, Issue in Progress

Nanomaterial catalyzed green synthesis of tetrazoles and its derivatives: a review on recent advancements

Abstract

Tetrazoles are indispensable nitrogen containing heterocyclic scaffolds that offer a broad spectrum of applications in various domains such as medicinal chemistry, high energy material science, biochemistry, pharmacology etc. Owing to their useful applications, a wide range of catalysts have been explored for green synthesis of tetrazole derivatives. In recent times, nanomaterials have been emerged as extremely efficient catalysts for different organic transformations because of their high surface area-to-volume ratio, easy surface modification, simple fabrications, easy recovery and reusability. In this article, we have presented an overview of utilization of various nano-catalysts, nanocomposites and other solid-supported nanomaterials as an efficient environmental benign catalytic system for green synthesis of tetrazoles and derivatives. This review will provide an exclusive emphasis on boehmite, magnetic, copper, carbon, MCM-41, and composite based nanomaterials that have been developed since the year 2010 for the synthesis of tetrazole derivatives. In addition, we have briefly discussed the fabrication, functionalization and characterization of some novel nanomaterials and their advantages in the synthesis of tetrazole and its derivatives along with the reaction mechanism that involves synthesis of tetrazole derivatives via nanomaterials catalysed reactions.

Graphical abstract: Nanomaterial catalyzed green synthesis of tetrazoles and its derivatives: a review on recent advancements

Article information

Article type
Review Article
Submitted
06 Aug 2021
Accepted
11 Nov 2021
First published
07 Dec 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 39058-39086

Nanomaterial catalyzed green synthesis of tetrazoles and its derivatives: a review on recent advancements

S. Swami, S. N. Sahu and R. Shrivastava, RSC Adv., 2021, 11, 39058 DOI: 10.1039/D1RA05955F

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