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Facile Rh(III)-Catalyzed Synthesis of Fluorinated Pyridines
[Image: see text] A Rh(III)-catalyzed C–H functionalization approach was developed for the preparation of multi-substituted 3-fluoropyridines from α-fluoro-α,β-unsaturated oximes and alkynes. Oximes substituted with aryl, heteroaryl and alkyl β-substituents were effective coupling partners, as were...
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| 發表在: | Org Lett |
|---|---|
| Main Authors: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2015
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4477688/ https://ncbi.nlm.nih.gov/pubmed/25992591 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.orglett.5b00979 |
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