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Iodine-mediated oxythiolation of o-vinylanilides with disulfides for the synthesis of benzoxazines
An efficient iodine-mediated oxythiolation of o-vinylanilides with disulfides was developed. By virtue of this method, a series of thio-tethered benzoxazine derivatives were synthesized in good to excellent yields. The reaction features high yields, is metal-free, and has a wide substrate scope.
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Royal Society of Chemistry
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982212/ https://www.ncbi.nlm.nih.gov/pubmed/35424675 http://dx.doi.org/10.1039/d2ra01078j |