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http://hdl.handle.net/123456789/3211Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Mandal, S.K. | - |
| dc.date.accessioned | 2020-12-18T08:18:08Z | - |
| dc.date.available | 2020-12-18T08:18:08Z | - |
| dc.date.issued | 2020 | - |
| dc.identifier.citation | Asian Journal of Organic Chemistry, 9(8), pp.1199-1204. | en_US |
| dc.identifier.other | https://doi.org/10.1002/ajoc.202000239 | - |
| dc.identifier.uri | https://onlinelibrary.wiley.com/doi/abs/10.1002/ajoc.202000239 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/3211 | - |
| dc.description | Only IISERM authors are available in the record. | - |
| dc.description.abstract | A one‐pot annulation of 1‐arylindazolones and acrylates is achieved through Ru(II)‐catalyzed sequential ortho‐alkenylation followed by oxidative intramolecular aza‐Michael addition reaction to deliver substituted indazolo[1,2‐a]indazolylidenes in good‐to‐excellent yields. The strategy showcased high functional group tolerance and the directing group ability of indazolone moiety was established for Csp2‐H bond activation. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Wiley-VCH Verlag | en_US |
| dc.subject | C−H Activation | en_US |
| dc.subject | Transition-metals | en_US |
| dc.subject | Acrylates | en_US |
| dc.subject | Catalysis | en_US |
| dc.subject | Cyclization | en_US |
| dc.title | Indazolone‐Assisted Sequential ortho‐Alkenylation‐Oxidative Aza‐Michael Addition of 1‐Arylindazolone Using Acrylates Under Ru(II) Catalysis | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Research Articles | |
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| File | Description | Size | Format | |
|---|---|---|---|---|
| Need to add pdf.odt | 8.63 kB | OpenDocument Text | View/Open |
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