Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/14228
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dc.contributor.authorSarothiya, Durgeshen_US
dc.contributor.authorKshirsagar, Umesh Achyutraoen_US
dc.date.accessioned2024-08-14T10:23:44Z-
dc.date.available2024-08-14T10:23:44Z-
dc.date.issued2024-
dc.identifier.citationSarothiya, D., & Kshirsagar, U. (2024). Oxidative Cross-Dehydrogenative C-H Bond Amination of Imidazo[1,2-a]pyridines in Aqueous Media Under Metal-free Conditions. Synthesis (Germany). https://doi.org/10.1055/a-2348-4764en_US
dc.identifier.issn0039-7881-
dc.identifier.otherEID(2-s2.0-85196860090)-
dc.identifier.urihttps://doi.org/10.1055/a-2348-4764-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/14228-
dc.description.abstractThe metal-free direct oxidative cross-dehydrogenative C-H bond amination of imidazopyridines with pyrazole in water as solvent has been developed under K2S2O8-promoted mild conditions. This strategy applies to variable imidazoheterocycles to give amination products in moderate to good yield. The described protocol also offers scale-up synthesis for the construction of C-N bonds, which makes it suitable for the synthesis of biologically active compounds and pharmaceuticals. © 2024 Georg Thieme Verlag. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherGeorg Thieme Verlagen_US
dc.sourceSynthesis (Germany)en_US
dc.subjectCDCen_US
dc.subjectGreen solventen_US
dc.subjectHeterocyclesen_US
dc.subjectMetal Freeen_US
dc.subjectOxidative couplingen_US
dc.titleOxidative Cross-Dehydrogenative C-H Bond Amination of Imidazo[1,2-a]pyridines in Aqueous Media Under Metal-free Conditionsen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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