Catalyst-Free One-Pot Tandem Reduction of Oxo and Ene/Yne Functionalities by Hydrazine: Synthesis of Substituted Oxindoles from Isatins

dc.contributor.authorJha, Anil
dc.date.accessioned2021-10-17T13:58:16Z
dc.date.available2021-10-17T13:58:16Z
dc.date.issued2014-04-15
dc.description.abstractAn unprecedented hydrazine-mediated tandem reduction of oxo and N-ene/yne functionalities of substituted isatins is reported to access various oxindoles. The reaction is performed by treating N-(2-alkenyl)/propargylisatins with hydrazine hydrate under catalyst-free refluxing conditions. The reduction proceeds efficiently without the aid of any catalyst at ambient pressure.en_US
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201402038
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2883
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectCatalyst-Freeen_US
dc.subjectSynthesisen_US
dc.subjectOxindolesen_US
dc.titleCatalyst-Free One-Pot Tandem Reduction of Oxo and Ene/Yne Functionalities by Hydrazine: Synthesis of Substituted Oxindoles from Isatinsen_US
dc.typeArticleen_US

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