Journal
CHEMISTRY-A EUROPEAN JOURNAL
Volume 27, Issue 24, Pages 7094-7098Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.202100763
Keywords
Aldehyde; arylnitrile; copper; α -hydroxy ketone; reductive cross-coupling
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Funding
- JSPS KAKENHI [JP18H01971, JP17H06449]
- Kanazawa University SAKIGAKE project 2020
- JST, PRESTO [JPMJPR19T2]
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This study presents a novel approach for the chemoselective synthesis of alpha-hydroxy ketones through a reductive cross-coupling reaction between aromatic aldehydes and arylnitriles using a copper catalyst and a silylboronate as a reductant.
A reductive cross-coupling reaction between aromatic aldehydes and arylnitriles using a copper catalyst and a silylboronate as a reductant is reported. This protocol represents an unprecedented approach to the chemoselective synthesis of alpha-hydroxy ketones by electrophile-electrophile cross-coupling.
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