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Simple Sulfinate Synthesis Enables C–H Trifluoromethylcyclopropanation
A simple method to convert readily available carboxylic acids into sulfinate salts employing an interrupted Barton decarboxylation reaction is reported. A medicinally oriented panel of ten new sulfinate reagents was created using this method, including a key trifluoromethylcyclopropanation reagent T...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4186797/ https://ncbi.nlm.nih.gov/pubmed/25088979 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/anie.201406622 |
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