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Nickel-Catalyzed Decarboxylative C–Si Bond Formation: A Regioselective Cross-Coupling Between Trialkyl Silanes and α,β-Unsaturated Carboxylic Acids

dc.contributor.authorAllam B.K.; Azeez S.; Kandasamy J.
dc.date.accessioned2025-05-24T09:40:11Z
dc.description.abstractThis 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.doihttps://doi.org/10.1002/aoc.5192
dc.identifier.urihttp://172.23.0.11:4000/handle/123456789/18911
dc.relation.ispartofseriesApplied Organometallic Chemistry
dc.titleNickel-Catalyzed Decarboxylative C–Si Bond Formation: A Regioselective Cross-Coupling Between Trialkyl Silanes and α,β-Unsaturated Carboxylic Acids

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