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dc.contributor.authorROZAS, ISABELen
dc.contributor.authorDIEZ CECILIA, ELENAen
dc.contributor.authorKELLY, BRENDANen
dc.date.accessioned2011-11-15T15:40:16Z
dc.date.available2011-11-15T15:40:16Z
dc.date.issued2011en
dc.date.submitted2011en
dc.identifier.citationElena Diez-Cecilia, Brendan Kelly, Isabel Rozas, One-step double reduction of aryl nitro and carbonyl groups using hydrazine, Tetrahedron Letters, 52, 50, 2011, 6702-6704en
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.description.abstractSingle-step reduction of aryl nitro and carbonyl groups to the corresponding synthetically useful alkyl-anilines occurs with excellent yields by treatment with hydrazine and a base in a solvent-free reaction. The method has been applied to a broad range of compounds with different properties. Investigations into the mechanism of the reduction reveal that each group is reduced independently. A mechanism is proposed for this novel reduction of aromatic nitro groups.en
dc.description.sponsorshipThe authors are grateful to IRCSET (E.D.C.) and HEAPRTLI-5 (B.K.) for financial support, and are indebted to Dr. John O?Brien for NMR studies.en
dc.format.extent6702-6704en
dc.language.isoenen
dc.relation.ispartofseriesTetrahedron Lettersen
dc.relation.ispartofseries52en
dc.relation.ispartofseries50en
dc.rightsYen
dc.subjectPhysical chemistryen
dc.subjectcarbonylen
dc.subjectaryl nitroen
dc.titleOne-step double reduction of aryl nitro and carbonyl groups using hydrazineen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/rozasien
dc.identifier.peoplefinderurlhttp://people.tcd.ie/kellyb12en
dc.identifier.rssinternalid75311en
dc.identifier.rssurihttp://dx.doi.org/10.1016/j.tetlet.2011.09.112en
dc.contributor.sponsorIrish Research Council for Science and Engineering Technology (IRCSET)en
dc.contributor.sponsorHigher Education Authority (HEA)en
dc.identifier.urihttp://hdl.handle.net/2262/60702


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