Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10154
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dc.contributor.authorNAIR, PADMAVATHY V. K.en_US
dc.contributor.authorSWAMI, GOURISHANKAR B.en_US
dc.contributor.authorGNANAPRAKASAM, BOOPATHYen_US
dc.date.accessioned2025-06-12T06:04:22Z-
dc.date.available2025-06-12T06:04:22Z-
dc.date.issued2025-04en_US
dc.identifier.citationOrganic Letters, 27(14), 3560–3565.en_US
dc.identifier.issn1523-7060en_US
dc.identifier.issn1523-7052en_US
dc.identifier.urihttps://doi.org/10.1021/acs.orglett.5c00600en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10154-
dc.description.abstractHerein, we report a RuH2(CO)(PPh3)3 catalyzed direct amidation of alcohols using readily available nitro compounds via a catalytic borrowing hydrogen method. This reaction proceeded via cascade reactions, including oxidation of alcohol, reduction of nitro group and formation of amides under one-pot condition. This protocol provides a single catalytic system for many reactions, a step economic advantage over the available techniques, tolerates various functionalities, and was demonstrated with broad substrate scope (47 examples).en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectAlcoholsen_US
dc.subjectAmidesen_US
dc.subjectAminesen_US
dc.subjectCatalystsen_US
dc.subjectOrganic compoundsen_US
dc.subject2025en_US
dc.titleDirect Synthesis of Amides from Nitro Compounds and Alcohols via Borrowing Hydrogenationen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic Lettersen_US
dc.publication.originofpublisherForeignen_US
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