| dc.contributor.author | Jha, Anil | |
| dc.date.accessioned | 2021-10-17T13:58:16Z | |
| dc.date.available | 2021-10-17T13:58:16Z | |
| dc.date.issued | 2014-04-15 | |
| dc.identifier.uri | https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201402038 | |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2883 | |
| dc.description.abstract | An 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.language.iso | en | en_US |
| dc.publisher | Wiley | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Catalyst-Free | en_US |
| dc.subject | Synthesis | en_US |
| dc.subject | Oxindoles | en_US |
| dc.title | Catalyst-Free One-Pot Tandem Reduction of Oxo and Ene/Yne Functionalities by Hydrazine: Synthesis of Substituted Oxindoles from Isatins | en_US |
| dc.type | Article | en_US |
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