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A Review On 1,2,4-Triazoles

Authors: Kishor Raval*, Kaushik Patel, Shivani Patel, Ronak Patel, Snehal Patel;

A Review On 1,2,4-Triazoles

Abstract

ABSTRACT Triazole is a five membered heterocyclic system consisting of two carbon atoms and three nitrogen atoms shows wide range of biological activities. Triazoles can be synthesized using Einhorn-Brunner reaction or the Pellizzari reaction from acyl hydrazides and various different method. Triazole derivatives are showing very promising and excellent therapeutic effectiveness. The major activities exhibited by these derivatives include insecticial, antifungal, antiviral, antibacterial, sedative,hypnotic, anticonvulsant and anti-inflammatory action. In recent year heterocyclic compounds analogues and derivatives have attracted strong interest due to their useful biological and pharmacological properties. The small and simple triazole nucleus is present in compounds involved in research aimed at evaluating new products that possess biological activities, such as,anti-microbial, anti-tumor, anthelmintic, anti-leishmanial, anti-convulsant and anti-inflammatory. Key words: Triazole, 1H-1, 2,4-Triazole, Heterocycle, Total synthesis, Biological activities.

Keywords

Key words: Triazole, 1H-1, 2,4-Triazole, Heterocycle, Total synthesis, Biological activities.

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selected citations
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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