Synthesis, structural analysis, and photophysical properties of bi-1,2,3-triazoles

Santana-Martínez, Ivette; Ramírez-Palma, María Teresa; Sánchez-Escalera, Javier; Martı́nez-Otero, Diego; García‐Eleno, Marco A.; Dorazco‐González, Alejandro; Cuevas-Yáñez, Erick

doi:10.1007/s11224-019-01390-1

Cited by 4 publications

(1 citation statement)

References 39 publications

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“…[36] It was also reported for some bis-triazoles the ability to be photoluminescent. [37] Finally, in 2008 Ackermann reported the formation of 1,4,5trisubstituted 1,2,3-triazoles 23 containing an aryl group at the C-5 position (Scheme 4). [38] The reaction conditions (0.1 equiv, CuI, 2 equiv.…”

Section: The Copper Catalyzed Azide Alkyne Cycloaddition (Cuaac) and ...mentioning

confidence: 99%

Each Interruption is an Opportunity: Novel Synthetic Strategies Explored Through Interrupted Click Reactions

Brunelli,

Russo,

Giustiniano

et al. 2024

Chemistry A European J

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The particular and unique mechanism of the copper‐catalyzed reaction between azides and alkynes (CuAAC) has not only allowed for the efficient synthesis of 1,2,3‐trisubstituted 1,4‐triazoles in excellent yields and under mild conditions, becoming the quintessential click reaction, but it has also enabled the straightforward formation of a metallocycle intermediate, the copper triazolyl. This, under suitable reaction conditions able to suppress its protonolysis, can be used either for the creation of new bicyclic triazolyl structures or for the generation of novel three or four‐component reactions. The aim of this review is to rationalize and unify all these transformations, which are collectively referred to as “interrupted click reactions”.

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Section: The Copper Catalyzed Azide Alkyne Cycloaddition (Cuaac) and ...mentioning

confidence: 99%

Each Interruption is an Opportunity: Novel Synthetic Strategies Explored Through Interrupted Click Reactions

Brunelli,

Russo,

Giustiniano

et al. 2024

Chemistry A European J

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Crystal structures and study of interaction mode of bis-benzimidazole-benzene derivatives with DNA

Valdes‐García

Viviano-Posadas

Rivera‐Chávez

et al. 2022

Journal of Molecular Structure

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Atropisomerism in bi-1,2,3-triazoles: Detection by 1H NMR using chiral shift reagents and torsional barriers calculations

Santana-Martínez

Bautista-Renedo²,

Ayala-Bueno³

et al. 2022

Journal of Molecular Structure

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Synthesis, structural analysis, and photophysical properties of bi-1,2,3-triazoles

Cited by 4 publications

References 39 publications

Each Interruption is an Opportunity: Novel Synthetic Strategies Explored Through Interrupted Click Reactions

Each Interruption is an Opportunity: Novel Synthetic Strategies Explored Through Interrupted Click Reactions

Crystal structures and study of interaction mode of bis-benzimidazole-benzene derivatives with DNA

Atropisomerism in bi-1,2,3-triazoles: Detection by 1H NMR using chiral shift reagents and torsional barriers calculations

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