Arylcarboxylation/Cyclization/Hydrogenation Cascade of Arylalkynes with Formate: Synthesis of Ester-Substituted Dioxodihydrodibenzothiazepine Derivatives

Abstract A novel method has been developed for the arylcarboxylation/cyclization/hydrogenation cascade reaction of arylalkynes with cheap and readily available sodium formate (HCO2Na). This approach facilitates the efficient synthesis of ester-substituted dioxodihydrodibenzothiazepine derivatives in the absence of photocatalysts and transition metals. The methodology features a broad substrate scope, operational simplicity, excellent functional group tolerance, mild reaction conditions, and scalability. Mechanistic experiments proved that the reaction involves a pathway that includes the formation of the carbon dioxide radical anion (CO2•–) from formate. Meanwhile, the hydrogen in the product comes from trace amounts of water in the solvent or HCO2Na.

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Publication Details

Journal
Organic Letters
Published
2026-09-19
DOI
https://doi.org/10.1021/acs.orglett.6c03505
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
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Arylcarboxylation/Cyclization/Hydrogenation Cascade of Arylalkynes with Formate: Synthesis of Ester-Substituted Dioxodihydrodibenzothiazepine Derivatives

Zhaoxin Wei, Chenjiang Liu, Ziren Chen, Bin Wang et al.
Organic Letters
Carbon dioxide utilization in catalysis
article

Arylcarboxylation/Cyclization/Hydrogenation Cascade of Arylalkynes with Formate: Synthesis of Ester-Substituted Dioxodihydrodibenzothiazepine Derivatives

Zhaoxin Wei, Chenjiang Liu, Ziren Chen, Bin Wang, Tao Zhang, Yonghong Zhang, Yu Xia, Shaofeng Wu, Weiwei Jin, Fei Xue
article en

Abstract

Abstract A novel method has been developed for the arylcarboxylation/cyclization/hydrogenation cascade reaction of arylalkynes with cheap and readily available sodium formate (HCO2Na). This approach facilitates the efficient synthesis of ester-substituted dioxodihydrodibenzothiazepine derivatives in the absence of photocatalysts and transition metals. The methodology features a broad substrate scope, operational simplicity, excellent functional group tolerance, mild reaction conditions, and scalability. Mechanistic experiments proved that the reaction involves a pathway that includes the formation of the carbon dioxide radical anion (CO2•–) from formate. Meanwhile, the hydrogen in the product comes from trace amounts of water in the solvent or HCO2Na.

Organic Letters
Xinjiang Normal University (CN), China Jiliang University (CN), Xinjiang University (CN)
Clean water and sanitation
Openalex Percentile: Top 24%
Carbon dioxide utilization in catalysis
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Arylcarboxylation/Cyclization/Hydrogenation Cascade of Arylalkynes with Formate: Synthesis of Ester-Substituted Dioxodihydrodibenzothiazepine Derivatives — Zhaoxin Wei, Chenjiang Liu, et al. · Organic Letters (2026) | TGRS Research Map | TGRS