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dc.contributor.authorPradhan, S.-
dc.contributor.authorDas, S.-
dc.contributor.authorKumar, G.-
dc.contributor.authorChatterjee, I.-
dc.date.accessioned2022-07-24T09:51:45Z-
dc.date.available2022-07-24T09:51:45Z-
dc.date.issued2022-07-24-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/3733-
dc.description.abstractThe unique property of hexafluoroisopropanol (HFIP) enables the regioselective hydroamination of 1,3-dienes with nitrogen heterocycles in a Markovnikov manner in the presence of catalytic Brønsted acid. This transition-metal-free intermolecular hydroamination protocol is achieved under mild reaction conditions. The aggregation by HFIP and Brønsted acid helps to activate the terminal double bond regioselectively. Following the protonation of diene, the C–N bond formation is accomplished upon the involvement of heterocyclic amines.en_US
dc.language.isoen_USen_US
dc.subjectHeterocyclic compoundsen_US
dc.subjectNitrogenen_US
dc.subjectOrganic reactionsen_US
dc.subjectReaction mechanismsen_US
dc.subjectSelectivityen_US
dc.titleThermodynamics analysis of an atmospheric water harvesting systemen_US
dc.typeArticleen_US
Appears in Collections:Year-2022

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