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dc.contributor.authorRahul, P-
dc.contributor.authorThomas, J-
dc.contributor.authorDehaen, W-
dc.contributor.authorJohn, J-
dc.date.accessioned2023-11-04T12:12:35Z-
dc.date.available2023-11-04T12:12:35Z-
dc.date.issued2022-12-30-
dc.identifier.citationMolecules;28(1): Article ID: 308en_US
dc.identifier.urihttps://doi.org/10.3390/molecules28010308-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/4581-
dc.description.abstractThe present review narrates several reports which deal with the synthesis of fused 1,2,3-triazole containing scaffolds following a sequential multicomponent reaction (MCR)—intramolecular azide-alkyne cycloaddition (IAAC) approach. The reviewed reactions were cleverly designed so as to incorporate azide and alkyne functionalities in the MCR product which was then subjected to IAAC. The review is divided into two sections based on the number of components in the multicomponent reaction. We have aimed at a critical discussion and also have highlighted either advantages or disadvantages of each methodologyen_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.subject1,2,3-triazoleen_US
dc.subjectmulticomponent reactionen_US
dc.subjectintramolecular azide-alkyne cycloadditionen_US
dc.subjectdipolar cycloadditionen_US
dc.titleAdvances in the Synthesis of Fused 1,2,3-Triazoles via a MCR-Intramolecular Azide-Alkyne Cycloaddition Approachen_US
dc.typeArticleen_US
Appears in Collections:2023

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