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Regioselective palladium-catalyzed ring-opening reactions of C1-substituted oxabicyclo[2,2,1]hepta-2,5-diene-2,3-dicarboxylates
Palladium-catalyzed ring-opening reactions of C1 substituted 7-oxanorbornadiene derivatives with aryl iodides were investigated. The optimal conditions for this reaction were found to be PdCl(2)(PPh(3))(2), ZnCl(2), Et(3)N and Zn in THF. Both steric and electronic factors played a role in the outcom...
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| Yayımlandı: | Beilstein J Org Chem |
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| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Beilstein-Institut
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4778517/ https://ncbi.nlm.nih.gov/pubmed/26977182 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.12.25 |
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