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.
Authors
- Hyun‐Joon Ha (ORCID: https://orcid.org/0000-0002-4651-9700)
- Eun Joo Kang (ORCID: https://orcid.org/0000-0002-7600-3609)
- Annaram Thirupathi
- Kwang‐Hyun Ahn (ORCID: https://orcid.org/0000-0002-2812-4895)
- Junhyeon Choi (ORCID: https://orcid.org/0009-0000-2812-8370)
- Ji Sung Kim (ORCID: https://orcid.org/0000-0003-2363-5060)
Institutions
- Kyung Hee University (KR)
- Hankuk University of Foreign Studies (KR)
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
Funders
- Ministry of Science and ICT, South Korea