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Catalytic Diastereo- and Enantioselective Fluoroamination of Alkenes
The stereoselective synthesis of syn-β-fluoroaziridine building blocks via chiral aryl iodide-catalyzed fluorination of allylic amines is reported. The method employs HF-pyridine as a nucleophilic fluoride source together with mCPBA as a stoichiometric oxidant, and affords access to arylethylamine d...
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| Опубликовано в: : | J Am Chem Soc |
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| Главные авторы: | , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2018
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5902804/ https://ncbi.nlm.nih.gov/pubmed/29583001 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jacs.8b02143 |
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