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A general, enantioselective synthesis of β- and γ-fluoroamines
In this Letter, we describe a short, high yielding protocol for the enantioselective (87–96% ee) and general synthesis of β-fluoroamines and previously difficult to access γ-fluoroamines from commercial aldehydes via organocatalysis.
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3769685/ https://ncbi.nlm.nih.gov/pubmed/24039308 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tetlet.2013.04.116 |
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