| dc.contributor.author |
Kumar, Dalip |
|
| dc.date.accessioned |
2021-10-27T04:18:38Z |
|
| dc.date.available |
2021-10-27T04:18:38Z |
|
| dc.date.issued |
2020-03-11 |
|
| dc.identifier.uri |
https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.202000013 |
|
| dc.identifier.uri |
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3013 |
|
| dc.description.abstract |
Substrate or solvent controlled regioselective C3, C5, and C8 arylation of quinolin-4(1H)-ones with diaryliodonium salts have been successfully achieved in high yields (up to 96 %). These protocols are applicable to a wide range of quinolone related heterocycles and provide potential access to naturally occurring benzoxocine and aaptamine analogues |
en_US |
| dc.language.iso |
en |
en_US |
| dc.publisher |
Wiley |
en_US |
| dc.subject |
Chemistry |
en_US |
| dc.subject |
Diaryliodonium Salts |
en_US |
| dc.subject |
Benzoxocine |
en_US |
| dc.subject |
Aaptamine Analogues |
en_US |
| dc.title |
Substrate or Solvent-Controlled PdII-Catalyzed Regioselective Arylation of Quinolin-4(1H)-ones Using Diaryliodonium Salts: Facile Access to Benzoxocine and Aaptamine Analogues |
en_US |
| dc.type |
Article |
en_US |