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Enantioselective benzylic C–H arylation via photoredox and nickel dual catalysis
The asymmetric cross-coupling reaction is developed as a straightforward strategy toward 1,1-diaryl alkanes, which are a key skeleton in a series of natural products and bioactive molecules in recent years. Here we report an enantioselective benzylic C(sp(3))−H bond arylation via photoredox/nickel d...
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| Foilsithe in: | Nat Commun |
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| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Nature Publishing Group UK
2019
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6685991/ https://ncbi.nlm.nih.gov/pubmed/31391466 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-019-11392-6 |
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