2022
DOI: 10.1016/j.inoche.2022.109524
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Copper (I)-catalyzed ‘Quick Click’ generated 1,2,3-triazole anthraquinone linkers for selective detection of Fe (II) ions

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Cited by 10 publications
(2 citation statements)
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“…This resulted in the formation of 1,4-disubstituted 1,2,3-triazoles, addressing the drawbacks of Huisgen cycloaddition. [92][93][94][95] The synthesis of triazoles can be approached from a sustainable development perspective. In this context, the careful selection of an appropriate catalyst is crucial for achieving efficient and environmentfriendly processes.…”
Section: Catalystmentioning
confidence: 99%
“…This resulted in the formation of 1,4-disubstituted 1,2,3-triazoles, addressing the drawbacks of Huisgen cycloaddition. [92][93][94][95] The synthesis of triazoles can be approached from a sustainable development perspective. In this context, the careful selection of an appropriate catalyst is crucial for achieving efficient and environmentfriendly processes.…”
Section: Catalystmentioning
confidence: 99%
“…The synthesis of 1,2,3triazole-based sensors involves the modification of the 1,2,3triazole ring to introduce functional groups that can interact with metal ions. 14 The improvement can be achieved through synthetic routes, including "click" chemistry, 9,[15][16][17] azidealkyne cycloaddition, 18,19 and Sonogashira coupling reactions. [20][21][22] "Click" chemistry is a powerful tool for synthesizing 1,2,3-triazole-based sensors.…”
Section: Introductionmentioning
confidence: 99%