One-Pot Aryl C–H Lactonization with CO2 via C–H Borylation and ZnEt2-Promoted C–B Bond Carboxylation

Abstract A one-pot, two-step strategy has been developed for the synthesis of dibenzopyranones via aryl C–H lactonization of 2-arylphenols with CO2. This method combines BBr3-mediated C–H borylation with ZnEt2-promoted C–B bond carboxylation, enabling the efficient construction of lactone frameworks. The reaction exhibits excellent functional group tolerance and is amenable to gram-scale synthesis, providing a range of dibenzopyranone derivatives in moderate to high yields.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-09-28
DOI
https://doi.org/10.1021/acs.joc.6c02130
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

One-Pot Aryl C–H Lactonization with CO2 via C–H Borylation and ZnEt2-Promoted C–B Bond Carboxylation

Baiquan Wang, Bin Li, Yongxin Zhang, Zezhao Liu
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
article

One-Pot Aryl C–H Lactonization with CO2 via C–H Borylation and ZnEt2-Promoted C–B Bond Carboxylation

Baiquan Wang, Bin Li, Yongxin Zhang, Zezhao Liu
article en

Abstract

Abstract A one-pot, two-step strategy has been developed for the synthesis of dibenzopyranones via aryl C–H lactonization of 2-arylphenols with CO2. This method combines BBr3-mediated C–H borylation with ZnEt2-promoted C–B bond carboxylation, enabling the efficient construction of lactone frameworks. The reaction exhibits excellent functional group tolerance and is amenable to gram-scale synthesis, providing a range of dibenzopyranone derivatives in moderate to high yields.

The Journal of Organic Chemistry
Chinese Academy of Sciences (CN), Nankai University (CN), Shanghai Institute of Organic Chemistry (CN)
Openalex Percentile: Top 22%
Catalytic C–H Functionalization Methods
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