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Preparation of cyclic imides from alkene-tethered amides: application of homogeneous Cu(ii) catalytic systems
A Cu-based homogeneous catalytic system was proposed for the preparation of imides from alkene-tethered amides. Here, O(2) acted as a terminal oxidant and a cheap and easily available oxygen source. The cleavage of C[double bond, length as m-dash]C bonds and the formation of C–N bonds were catalyzed...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049870/ https://www.ncbi.nlm.nih.gov/pubmed/35492186 http://dx.doi.org/10.1039/c9ra10422d |
Sumario: | A Cu-based homogeneous catalytic system was proposed for the preparation of imides from alkene-tethered amides. Here, O(2) acted as a terminal oxidant and a cheap and easily available oxygen source. The cleavage of C[double bond, length as m-dash]C bonds and the formation of C–N bonds were catalyzed by Cu(ii) salts with proper nitrogen-containing ligands under 100 °C. The synthesis approach has potential applications in pharmaceutical syntheses. Moreover, scaled-up experiments confirmed the practical applicability. |
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