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Imidazolidin-4-ones via (3+2) cycloadditions of aza-oxyallyl cations onto (E)-Narylideneanilines
In the course of our studies on the chemistry of oxyallyl species we uncovered a new (3+2) cycloaddition of aza-oxyallyl systems, generated in situ from N-benzyloxy-2-chloroamides in the presence of NEt(3), onto N-arylimines yielding imidazolidin-4-ones in moderate to good yields. The cycloadditions...
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| Vydáno v: | Tetrahedron Lett |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6236675/ https://ncbi.nlm.nih.gov/pubmed/30449908 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tetlet.2018.08.056 |
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