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A novel approach to oxoisoaporphine alkaloids via regioselective metalation of alkoxy isoquinolines
Oxoisoaporphine alkaloids are conveniently prepared via direct ring metalation of alkoxy-substituted isoquinolines at C-1, followed by reaction with iodine. Subsequent Suzuki cross-coupling of the resulting 1-iodoisoquinolines to methyl 2-(isoquinolin-1-yl)benzoates and intramolecular acylation of t...
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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
2017
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5564254/ https://ncbi.nlm.nih.gov/pubmed/28904605 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.13.156 |
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