| dc.contributor.author |
Kumar, Anil |
|
| dc.date.accessioned |
2021-10-14T13:11:25Z |
|
| dc.date.available |
2021-10-14T13:11:25Z |
|
| dc.date.issued |
2017-11-09 |
|
| dc.identifier.uri |
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.201701379 |
|
| dc.identifier.uri |
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2829 |
|
| dc.description.abstract |
A modular synthesis of azepino-fused isoindolinones has been developed in form of a sequential copper- and palladium-catalyzed tandem reaction. The developed protocol involved the formation of one carbon–nitrogen and two carbon–carbon bonds in a one-pot fashion. The palladium-catalyzed intramolecular direct-arylation step involves the formation of an unusual eight-membered palladacycle. |
en_US |
| dc.language.iso |
en |
en_US |
| dc.publisher |
Wiley |
en_US |
| dc.subject |
Chemistry |
en_US |
| dc.subject |
Copper-Catalyzed |
en_US |
| dc.subject |
Sonogashira Coupling |
en_US |
| dc.subject |
Azepino-Fused Isoindolinones |
en_US |
| dc.title |
Sequential Copper-Catalyzed Sonogashira Coupling, Hydroamination and Palladium-Catalyzed Intramolecular Direct Arylation: Synthesis of Azepino-Fused Isoindolinones |
en_US |
| dc.type |
Article |
en_US |