(Bpin) <sub>2</sub> ‐Catalyzed Cycloaddition Reaction of Epoxides and Carbon Dioxide with a Broad Range of Functional Groups

Abstract Carbon dioxide (CO 2 ) fixation and utilization is a critical area of research for scientists, particularly in light of the escalating greenhouse effect. Among the various strategies being explored, the transformation of CO 2 into high‐value compounds is particularly advantageous. In this study, we report one general approach for synthesizing the cyclic carbonates from epoxides and carbon dioxide using Lewis acid catalysis, bis(pinacolato)diboron ((Bpin) 2 ), which is one commercial available, stable, and cost‐effective reagent. The cycloaddition reactions were conducted under mild conditions and demonstrated high yields while accommodating a wide range of broad functional groups. This methodology offers an economical and practical route for the synthesis of cyclic carbonates.

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Journal
ChemistrySelect
Published
2025-05-28
DOI
https://doi.org/10.1002/slct.202501786
Citations
1
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
0.70

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article

(Bpin) 2 ‐Catalyzed Cycloaddition Reaction of Epoxides and Carbon Dioxide with a Broad Range of Functional Groups

Wei‐Li Li, Xinghua Ma
1 citations
ChemistrySelect
Carbon dioxide utilization in catalysis
0.70
article

(Bpin) 2 ‐Catalyzed Cycloaddition Reaction of Epoxides and Carbon Dioxide with a Broad Range of Functional Groups

Wei‐Li Li, Xinghua Ma
article en
1 citations

Abstract

Abstract Carbon dioxide (CO 2 ) fixation and utilization is a critical area of research for scientists, particularly in light of the escalating greenhouse effect. Among the various strategies being explored, the transformation of CO 2 into high‐value compounds is particularly advantageous. In this study, we report one general approach for synthesizing the cyclic carbonates from epoxides and carbon dioxide using Lewis acid catalysis, bis(pinacolato)diboron ((Bpin) 2 ), which is one commercial available, stable, and cost‐effective reagent. The cycloaddition reactions were conducted under mild conditions and demonstrated high yields while accommodating a wide range of broad functional groups. This methodology offers an economical and practical route for the synthesis of cyclic carbonates.

ChemistrySelectVol. 10(21)
Ningbo University (CN)
Ningbo University, K. C. Wong Magna Fund in Ningbo University
Openalex Percentile: Top 36%
Carbon dioxide utilization in catalysis
0.70
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