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C–H functionalization of amines with aryl halides by nickel-photoredox catalysis
We describe the functionalization of α-amino C–H bonds with aryl halides using a combination of nickel and photoredox catalysis. This direct C–H, C–X coupling uses inexpensive and readily available starting materials to generate benzylic amines, an important class of bioactive molecules. Mechanistic...
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| Pubblicato in: | Chem Sci |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Royal Society of Chemistry
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5207500/ https://ncbi.nlm.nih.gov/pubmed/28058105 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/c6sc02815b |
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