| 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.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.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.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 |