Fe(II)-Iminopyridine Catalyst for the Regioselective Synthesis of Oxazolidinones Using Carbon Dioxide

This study presents the application of a novel Fe-iminopyridine catalyst for the regioselective synthesis of oxazolidinones from carbon dioxide and aziridines. Our findings demonstrate that the Fe-iminopyridine catalyst containing imidazole functional group offers promising efficiency and facilitates a sustainable approach to green chemical synthesis at 50 °C and 10 bar CO<sub>2</sub> pressure in a single-component Fe catalyst system. Various aziridines with carboxylic acid-derived substituents were transformed into 5-carbonyl substituted oxazolidinone products. The regioselective synthesis of oxazolidinones followed by the reduction enhances their utility for the pharmaceutically valuable compounds.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-12-04
DOI
https://doi.org/10.1021/acs.joc.4c01907
Citations
6
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
1.07

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article

Fe(II)-Iminopyridine Catalyst for the Regioselective Synthesis of Oxazolidinones Using Carbon Dioxide

Hyun‐Joon Ha, Eun Joo Kang, Annaram Thirupathi, Kwang‐Hyun Ahn et al.
6 citations
The Journal of Organic Chemistry
Carbon dioxide utilization in catalysis
1.07
article

Fe(II)-Iminopyridine Catalyst for the Regioselective Synthesis of Oxazolidinones Using Carbon Dioxide

Hyun‐Joon Ha, Eun Joo Kang, Annaram Thirupathi, Kwang‐Hyun Ahn, Junhyeon Choi, Ji Sung Kim
article en
6 citations

Abstract

This study presents the application of a novel Fe-iminopyridine catalyst for the regioselective synthesis of oxazolidinones from carbon dioxide and aziridines. Our findings demonstrate that the Fe-iminopyridine catalyst containing imidazole functional group offers promising efficiency and facilitates a sustainable approach to green chemical synthesis at 50 °C and 10 bar CO<sub>2</sub> pressure in a single-component Fe catalyst system. Various aziridines with carboxylic acid-derived substituents were transformed into 5-carbonyl substituted oxazolidinone products. The regioselective synthesis of oxazolidinones followed by the reduction enhances their utility for the pharmaceutically valuable compounds.

The Journal of Organic ChemistryVol. 89(24)
Kyung Hee University (KR), Hankuk University of Foreign Studies (KR)
Ministry of Science and ICT, South Korea
Openalex Percentile: Top 28%
Carbon dioxide utilization in catalysis
1.07
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