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Current Organic Synthesis

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ISSN (Online): 1875-6271

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Review Article

Emerging Aspects of Triazole in Organic Synthesis: Exploring its Potential as a Gelator

Author(s): Rabecca Jenifer Vasanthan, Sheersha Pradhan and Mohan Das Thangamuthu*

Volume 21, Issue 4, 2024

Published on: 29 December, 2022

Page: [456 - 512] Pages: 57

DOI: 10.2174/1570179420666221010094531

Price: $65

Abstract

Cu(I)-catalyzed azide−alkyne 1,3-dipolar cycloaddition (CuAAC) - commonly known as the “click reaction” - serves as the most effective and highly reliable tool for facile construction of simple to complex designs at the molecular level. It relates to the formation of carbon heteroatomic systems by joining or clicking small molecular pieces together with the help of various organic reactions such as cycloaddition, conjugate addition, ring-opening, etc. Such dynamic strategy results in the generation of triazole and its derivatives from azides and alkynes with three nitrogen atoms in the five-membered aromatic azole ring that often forms gel-assembled structures having gelating properties. These scaffolds have led to prominent applications in designing advanced soft materials, 3D printing, ion sensing, drug delivery, photonics, separation, and purification. In this review, we mainly emphasize the different mechanistic aspects of triazole formation, which includes the synthesis of sugar-based and non-sugar-based triazoles, and their gel applications reported in the literature for the past ten years, as well as the upcoming scope in different branches of applied sciences.

Keywords: Triazole, sugar-triazole, click chemistry, gelators, self-assembly, pyrrodiazoles.

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