Rhenium-catalyzed α-alkylation of enol acetates with α-alkyl-substituted β-diketones

When enol acetates were treated with α-alkyl-substituted β-diketones in the presence of a catalytic amount of a rhenium complex, such as ReBr(CO)5, the carbon–carbon bond formation proceeded by the elimination of β-dicarbonyl units of α-alkyl-substituted β-diketones to give the corresponding α-alkylated carbonyl compounds in moderate to good yields.

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Publication Details

Journal
Synlett
Published
2026-09-10
DOI
https://doi.org/10.1055/a-2954-8207
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
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article

Rhenium-catalyzed α-alkylation of enol acetates with α-alkyl-substituted β-diketones

Yutaka Nishiyama, S. Tsuda, Yuya Matsuda, Shinya Murakami
Synlett
Asymmetric Hydrogenation and Catalysis
article

Rhenium-catalyzed α-alkylation of enol acetates with α-alkyl-substituted β-diketones

Yutaka Nishiyama, S. Tsuda, Yuya Matsuda, Shinya Murakami
article en

Abstract

When enol acetates were treated with α-alkyl-substituted β-diketones in the presence of a catalytic amount of a rhenium complex, such as ReBr(CO)5, the carbon–carbon bond formation proceeded by the elimination of β-dicarbonyl units of α-alkyl-substituted β-diketones to give the corresponding α-alkylated carbonyl compounds in moderate to good yields.

Synlett
Kansai University (JP), Osaka Dental University (JP)
Openalex Percentile: Top 25%
Asymmetric Hydrogenation and Catalysis
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