| dc.contributor.author |
Sakhuja, Rajeev |
|
| dc.date.accessioned |
2021-11-11T10:58:36Z |
|
| dc.date.available |
2021-11-11T10:58:36Z |
|
| dc.date.issued |
2018-09-05 |
|
| dc.identifier.uri |
https://pubs.acs.org/doi/10.1021/acs.joc.8b01630 |
|
| dc.identifier.uri |
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3352 |
|
| dc.description.abstract |
A Rh(III)-catalyzed strategy involving the [4+1] annulation of 2-arylphthalazine-1,4-diones with α-diazo carbonyl compounds was developed, accessing a series of unprecedented hydroxy-dihydroindazolo-fused phthalazines in good to excellent yields. By varying the additive, phthalazino-fused cinnolines were synthesized under Rh-catalyzed conditions via [4+2] annulation between the same starting materials. Notably, such two strategies showed a good functional group tolerance and high atom efficiency. |
en_US |
| dc.language.iso |
en |
en_US |
| dc.publisher |
ACS |
en_US |
| dc.subject |
Chemistry |
en_US |
| dc.subject |
Additives |
en_US |
| dc.subject |
Addition reactions |
en_US |
| dc.subject |
Mixtures |
en_US |
| dc.title |
Additive-Driven Rhodium-Catalyzed [4+1]/[4+2] Annulations of N-Arylphthalazine-1,4-dione with α-Diazo Carbonyl Compounds |
en_US |
| dc.type |
Article |
en_US |