期刊
TETRAHEDRON
卷 91, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2021.132212
关键词
N-Heterocyclic carbene; Radical; Aldehyde; beta-Ketocarbonyls
资金
- JSPS KAKENHI [JP21H04681, JP17H06449, JP20J20599]
- Kanazawa University SAKIGAKE project
- JST, PRESTO [JPMJPR19T2]
The N-heterocyclic carbene-catalyzed radical cross-coupling between aldehydes and alpha-bromoesters or alpha-bromoamides allows for the synthesis of beta-ketocarbonyl compounds under mild reaction conditions. Both aromatic and aliphatic aldehydes can serve as suitable acyl donors by using appropriate NHC catalyst precursors.
N-Heterocyclic carbene-catalyzed radical cross-coupling between aldehydes and alpha-bromoesters or alpha-bromoamides is described. beta-Ketocarbonyl compounds having a quaternary carbon center at the alpha-position can be synthesized under mild reaction conditions. Both aromatic and aliphatic aldehydes are suitable acyl donors by employing proper NHC catalyst precursors. (C) 2021 Elsevier Ltd. All rights reserved.
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