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Optimized Synthesis of a Pentafluoro-gem-diol and Conversion to a CF(2)Br-Glucopyranose through Trifluoroacetate-Release and Halogenation
Pentafluoro-gem-diols are substrates that enable the synthesis of valuable difluoromethylene-containing organic molecules through the release of trifluoroacetate. Currently, only one synthetic strategy is available to assemble these important precursors. Herein, two new synthetic strategies to a com...
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| Vydáno v: | Tetrahedron Lett |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4863236/ https://ncbi.nlm.nih.gov/pubmed/27182091 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tetlet.2016.03.064 |
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