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Highly Diastereoselective and General Synthesis of Primary β-Fluoroamines
[Image: see text] A short, high yielding protocol has been developed for the highly diastereoselective (dr >20:1) and general synthesis of primary β-fluoroamines by the enantioselective α-fluorination of aldehydes, conversion into the N-sulfinyl aldimine, nucleophilic addition of various organome...
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| Hoofdauteurs: | , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2011
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3196525/ https://ncbi.nlm.nih.gov/pubmed/21942742 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol202415j |
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