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Corrole and nucleophilic aromatic substitution are not incompatible: a novel route to 2,3-difunctionalized copper corrolates
The insertion of a –NO(2) group onto the corrole framework represents a key step for subsequent synthetic manipulation of the macrocycle based on the chemical versatility of such a functionality. Here we report results on the investigation of a copper 3-NO(2)-triarylcorrolate in nucleophilic aromati...
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| I publikationen: | Org Biomol Chem |
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| Huvudupphovsmän: | , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2015
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4454397/ https://ncbi.nlm.nih.gov/pubmed/25986693 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/c5ob00659g |
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