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Hydrosilylation of Aldehydes and Ketones Catalyzed by Nickel PCP-Pincer Hydride Complexes
Nickel PCP-pincer hydride complexes catalyze chemoselective hydrosilylation of CO bonds of aldehydes and ketones in the presence of other functional groups. The mechanism involves CO insertion into a nickel−hydrogen bond, followed by cleavage of the newly formed Ni−O bond with a silane.
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Published in: | Organometallics 2009-01, Vol.28 (2), p.582-586 |
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Language: | English |
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cites | cdi_FETCH-LOGICAL-a325t-4a10f081b5af1f89b4f2ec227511b5b14209b483134eb7c5dbc44a58669817453 |
container_end_page | 586 |
container_issue | 2 |
container_start_page | 582 |
container_title | Organometallics |
container_volume | 28 |
creator | Chakraborty, Sumit Krause, Jeanette A Guan, Hairong |
description | Nickel PCP-pincer hydride complexes catalyze chemoselective hydrosilylation of CO bonds of aldehydes and ketones in the presence of other functional groups. The mechanism involves CO insertion into a nickel−hydrogen bond, followed by cleavage of the newly formed Ni−O bond with a silane. |
doi_str_mv | 10.1021/om800948f |
format | article |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
title | Hydrosilylation of Aldehydes and Ketones Catalyzed by Nickel PCP-Pincer Hydride Complexes |
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