Gold‐Catalyzed Heck and Suzuki‐Type Reactions: Challenges and Recent Advances

Abstract Transition metal‐catalyzed Suzuki and Heck reactions are two of the most common carbon‐carbon bond formation reactions. Gold, unlike other transition metals (Pd, Ni, and Cu), offers unique reactivity profiles, and has emerged as an efficient tool in the field of synthetic organic chemistry. This mini‐review focused on the recent work in gold‐catalyzed Heck and Suzuki‐type reactions, especially by photocatalysts or ligand design, which show reactivities and features distinct from other transition metals. These discoveries will further facilitate the development of gold redox catalysis as well as applications in organic synthesis, biochemistry, and medicinal chemistry.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-08-21
DOI
https://doi.org/10.1002/ejoc.202400793
Citations
4
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
1.00

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article

Gold‐Catalyzed Heck and Suzuki‐Type Reactions: Challenges and Recent Advances

Gang Li, Lizhu Zhang, Zhonghua Xia, Wenqian Du et al.
4 citations
European Journal of Organic Chemistry
Catalytic Alkyne Reactions
1.00
article

Gold‐Catalyzed Heck and Suzuki‐Type Reactions: Challenges and Recent Advances

Gang Li, Lizhu Zhang, Zhonghua Xia, Wenqian Du, Jiawen Wu
article en
4 citations

Abstract

Abstract Transition metal‐catalyzed Suzuki and Heck reactions are two of the most common carbon‐carbon bond formation reactions. Gold, unlike other transition metals (Pd, Ni, and Cu), offers unique reactivity profiles, and has emerged as an efficient tool in the field of synthetic organic chemistry. This mini‐review focused on the recent work in gold‐catalyzed Heck and Suzuki‐type reactions, especially by photocatalysts or ligand design, which show reactivities and features distinct from other transition metals. These discoveries will further facilitate the development of gold redox catalysis as well as applications in organic synthesis, biochemistry, and medicinal chemistry.

European Journal of Organic ChemistryVol. 27(45)
Beijing Institute of Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 27%
Catalytic Alkyne Reactions
1.00
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