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Nickel-catalyzed reductive cleavage of aryl alkyl ethers to arenes in absence of external reductant
The reductive cleavage of the C–O bonds of aryl ethers has great potential in organic synthesis. Although several catalysts that can promote the reductive cleavage of aryl ethers have been reported, all such systems require the use of an external reductant, e.g., hydrosilane or hydrogen. Here, we re...
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| Опубликовано в: : | Chem Sci |
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| Главные авторы: | , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Royal Society of Chemistry
2015
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5659071/ https://ncbi.nlm.nih.gov/pubmed/29511506 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/c5sc00305a |
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