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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2914
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dc.contributor.authorKumar, Anil-
dc.date.accessioned2021-10-27T04:09:17Z-
dc.date.available2021-10-27T04:09:17Z-
dc.date.issued2013-03-14-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1002/chin.201312119-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2914-
dc.description.abstractThe archetypical CuAAC click chemistry is explored to assemble diverse 3-(triazol-1-yl)methyl-imidazo[1,2-a]pyridines. The approach is simple, general, and environmentally benign to generate a library of novel triazolo-imidazo[1,2-a]pyridine derivatives in good yield (30–90%).en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectChemInformen_US
dc.subjectCuAAC Reactionen_US
dc.subjectSynthesisen_US
dc.titleChemInform Abstract: Exploration of the CuAAC Reaction for the Synthesis of Novel 3-(Triazol-1-yl)methyl-imidazo[1,2-a]pyridinesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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