Nickel-Catalyzed Decarboxylative C–Si Bond Formation: A Regioselective Cross-Coupling Between Trialkyl Silanes and α,β-Unsaturated Carboxylic Acids
| dc.contributor.author | Allam B.K.; Azeez S.; Kandasamy J. | |
| dc.date.accessioned | 2025-05-24T09:40:11Z | |
| dc.description.abstract | This report presents the first example of nickel-catalyzed mild decarboxylative cross-coupling reaction for the regioselective formation of C–Si bond. An easily accessible and significantly stable Ni (dmg)2 owes the role of key promoter. This reaction is highly functional group tolerant and offers α,β-unsaturated silanes in synthetically useful yields. The reaction gives access to the successful utilization of otherwise difficult trialkyl silanes as coupling partners and operates at a moderate temperature, which is beneficial to deal with highly volatile silanes. © 2019 John Wiley & Sons, Ltd. | |
| dc.identifier.doi | https://doi.org/10.1002/aoc.5192 | |
| dc.identifier.uri | http://172.23.0.11:4000/handle/123456789/18911 | |
| dc.relation.ispartofseries | Applied Organometallic Chemistry | |
| dc.title | Nickel-Catalyzed Decarboxylative C–Si Bond Formation: A Regioselective Cross-Coupling Between Trialkyl Silanes and α,β-Unsaturated Carboxylic Acids |