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Rhodium catalyzed synthesis of isoindolinones via C-H activation of N-benzoylsulfonamides
An efficient approach to a wide range of isoindolinones, including 3-monosubstituted and 3,3-disubstituted isoindolinones, from the annulation of N-benzoylsulfonamides with olefins and diazoacetate has been developed. The transformation is broadly compatible with both terminal and internal olefins....
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3472453/ https://ncbi.nlm.nih.gov/pubmed/23087489 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tet.2012.08.095 |
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