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GaCl(3)-Catalyzed Ring-Opening Carbonyl-Olefin Metathesis.
The development of a Lewis acid-catalyzed ring-opening cross-metathesis reaction which enables selective access to acyclic, unsaturated ketones as the carbonyl-olefin metathesis products is described. While catalytic amounts of FeCl(3) were previously identified as optimal to catalyze ring-closing m...
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| Vydáno v: | Org Lett |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6905395/ https://ncbi.nlm.nih.gov/pubmed/30052456 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.orglett.8b02086 |
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