Solvent‐Free Synthesis of Carvone Oxime Ester and Carvone Oxime Sulfonic Esters

Abstract A ZnO‐mediated benzoylation between carvone oxime and acyl is reported, enabling access to diverse carvone oxime ester and carvone oxime sulfonic esters under solvent‐free conditions. The operationally simple procedure provides a novel method for the synthesis of oxime‐ester bonds with excellent chemo selectivity. This strategy provides a mild, direct, and green approach for synthesizing carvone oxime ester in moderate to excellent yields with good substrate tolerance. In addition, carvone oxime was synthesized under solvent‐free conditions.

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Publication Details

Journal
ChemistrySelect
Published
2024-10-01
DOI
https://doi.org/10.1002/slct.202403018
Citations
2
Primary Topic
Chemistry and Chemical Engineering
Type
article
Field-Weighted Citation Impact
0.50
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Solvent‐Free Synthesis of Carvone Oxime Ester and Carvone Oxime Sulfonic Esters

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article

Solvent‐Free Synthesis of Carvone Oxime Ester and Carvone Oxime Sulfonic Esters

Hao Yang, Hao Yao, Xiaoying Liu, Jiayu Chen, Guo Zeng, Guanxiong Yan, Qingwen Gui, Hongmei Jiang
article en
2 citations

Abstract

Abstract A ZnO‐mediated benzoylation between carvone oxime and acyl is reported, enabling access to diverse carvone oxime ester and carvone oxime sulfonic esters under solvent‐free conditions. The operationally simple procedure provides a novel method for the synthesis of oxime‐ester bonds with excellent chemo selectivity. This strategy provides a mild, direct, and green approach for synthesizing carvone oxime ester in moderate to excellent yields with good substrate tolerance. In addition, carvone oxime was synthesized under solvent‐free conditions.

ChemistrySelectVol. 9(38)
Hunan Agricultural University (CN)
Openalex Percentile: Top 35%
Chemistry and Chemical Engineering
0.50
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