Straightforward synthesis of diarylacetylenes from tetrachloroethylene using Kumada coupling reaction by Pd catalyst. Application to tri- and tetraarylethylenes

Abstract Pd-catalyzed Kumada coupling reaction of tetrachloroethylene and Grignard reagents was effective for the formation of diarylacetylenes as simple and convenient reaction, in which diarylacetylenes were successfully obtained in up to 82% yields and 14 examples were demonstrated. In addition, the current reaction was applicable for the straightforward synthesis of tri and tetra-substituted arylethylenes in good yields.

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Publication Details

Journal
Bulletin of the Chemical Society of Japan
Published
2025-04-02
DOI
https://doi.org/10.1093/bulcsj/uoaf025
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
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article

Straightforward synthesis of diarylacetylenes from tetrachloroethylene using Kumada coupling reaction by Pd catalyst. Application to tri- and tetraarylethylenes

Yuta Fujiki, Norihito Kawashita, Junya Kikuzawa, Kouichi Matsumoto et al.
Bulletin of the Chemical Society of Japan
Chemical Synthesis and Reactions
article

Straightforward synthesis of diarylacetylenes from tetrachloroethylene using Kumada coupling reaction by Pd catalyst. Application to tri- and tetraarylethylenes

Yuta Fujiki, Norihito Kawashita, Junya Kikuzawa, Kouichi Matsumoto, Akane Togo, Kazuki Miyamoto
article en

Abstract

Abstract Pd-catalyzed Kumada coupling reaction of tetrachloroethylene and Grignard reagents was effective for the formation of diarylacetylenes as simple and convenient reaction, in which diarylacetylenes were successfully obtained in up to 82% yields and 14 examples were demonstrated. In addition, the current reaction was applicable for the straightforward synthesis of tri and tetra-substituted arylethylenes in good yields.

Bulletin of the Chemical Society of Japan
Kindai University (JP)
Openalex Percentile: Top 95%
Chemical Synthesis and Reactions
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