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Palladium-catalyzed ring-opening reactions of cyclopropanated 7-oxabenzonorbornadiene with alcohols
Palladium-catalyzed ring-opening reactions of cyclopropanated 7-oxabenzonorbornadiene derivatives using alcohol nucleophiles were investigated. The optimal conditions were found to be 10 mol % PdCl(2)(CH(3)CN)(2) in methanol, offering yields up to 92%. The reaction was successful using primary, seco...
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| 出版年: | Beilstein J Org Chem |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Beilstein-Institut
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5082584/ https://ncbi.nlm.nih.gov/pubmed/27829926 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.12.209 |
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