Iridium-catalyzed [4 + 2] annulation of 1-arylindazolones with α-diazo carbonyl compounds: access to indazolone-fused cinnolines
| dc.contributor.author | Sakhuja, Rajeev | |
| dc.date.accessioned | 2021-11-11T10:58:29Z | |
| dc.date.available | 2021-11-11T10:58:29Z | |
| dc.date.issued | 2018 | |
| dc.description.abstract | An efficient one-pot Ir-catalyzed method was developed for the synthesis of indazolone-fused cinnolines by [4 + 2] annulation of 1-arylindazolones with α-diazo carbonyl compounds via sequential C–H activation/carbene insertion/cyclization in a tandem manner. This method has excellent tolerance towards electron-withdrawing and electron-donating functional groups on 1-arylindazolone. This method was also found to be applicable to cyclic α-diazo carbonyl compounds. | en_US |
| dc.identifier.uri | https://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob01681j | |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3350 | |
| dc.language.iso | en | en_US |
| dc.publisher | RSC | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Iridium-catalyzed [4 + 2] | en_US |
| dc.subject | Indazolone-fused cinnolines | en_US |
| dc.title | Iridium-catalyzed [4 + 2] annulation of 1-arylindazolones with α-diazo carbonyl compounds: access to indazolone-fused cinnolines | en_US |
| dc.type | Article | en_US |
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