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Highly Regio- and Enantioselective Vicinal Dihalogenation of Allyl Amides
We report a highly regio-, diastereo- and enantioselective vicinal dihalogenation of allyl amides. E-and Z-alkenes with both aryl and alkyl substituents were compatible with this chemistry. This is the result of exquisite catalyst controlled regioselectivity enabling use of electronically unbiased s...
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| Veröffentlicht in: | J Am Chem Soc |
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| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7790169/ https://ncbi.nlm.nih.gov/pubmed/28112919 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jacs.6b09203 |
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