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Remote site-selective C–H activation directed by a catalytic bifunctional template
Converting C–H bonds directly into carbon-carbon and carbon-heteroatom bonds can significantly improve step-economy in synthesis by providing alternative disconnections to traditional functional group manipulations. In this context, directed C–H activation reactions have been extensively explored fo...
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| Veröffentlicht in: | Nature |
|---|---|
| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5477648/ https://ncbi.nlm.nih.gov/pubmed/28273068 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature21418 |
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