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Reactivity in the Nucleophilic Aromatic Substitution Reactions of Pyridinium Ions
The “element effect” in nucleophilic aromatic substitution reactions (S(N)Ar) is characterized by the leaving group order, L = F > NO(2) > Cl ≈ Br > I, in activated aryl substrates. A different leaving group order is observed in the substitution reactions of ring-substituted N-methylpyridin...
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| Hoofdauteurs: | , , , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2014
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4110164/ https://ncbi.nlm.nih.gov/pubmed/24995709 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/c4ob00946k |
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