Please use this identifier to cite or link to this item:
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4198Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | BISHT, GIRISH SINGH | en_US |
| dc.contributor.author | GNANAPRAKASAM, BOOPATHY | en_US |
| dc.date.accessioned | 2019-11-29T11:37:17Z | |
| dc.date.available | 2019-11-29T11:37:17Z | |
| dc.date.issued | 2019-09 | en_US |
| dc.identifier.citation | Journal of Organic Chemistry, 84(21), 13516-13527. | en_US |
| dc.identifier.issn | 1520-6904 | en_US |
| dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4198 | - |
| dc.identifier.uri | https://doi.org/10.1021/acs.joc.9b01771 | en_US |
| dc.description.abstract | A novel and efficient transition-metal-free approach for the exclusive synthesis of Z-3-(aminobenzylidene/aminoalkylidene)indolin-2-ones in high yield from 2-oxindole and aryl/alkyl nitrile in the presence of LiOtBu and 2,2?-bipyridine system is described. In addition, we disclosed a new approach towards the metal-free fluorination using selectfluor and the C?C bond cleavage using CuI and environmentally benign O2. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | American Chemical Society | en_US |
| dc.subject | Beta-Dicarbonyl|Compounds | en_US |
| dc.subject | One-Pot Synthesis | en_US |
| dc.subject | C Double-Bond | en_US |
| dc.subject | Heterocyclic Synthesis | en_US |
| dc.subject | Oxidative Cleavage | en_US |
| dc.subject | Coupling | en_US |
| dc.subject | TOC-NOV-2019 | en_US |
| dc.subject | 2019 | en_US |
| dc.title | Transition-Metal-Free Addition Reaction for the Synthesis of 3-(Aminobenzylidene/aminoalkylidene)indolin-2-ones and Its Synthetic Applications | en_US |
| dc.type | Article | en_US |
| dc.contributor.department | Dept. of Chemistry | en_US |
| dc.identifier.sourcetitle | Journal of Organic Chemistry | en_US |
| dc.publication.originofpublisher | Foreign | en_US |
| Appears in Collections: | JOURNAL ARTICLES | |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.