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Temperature-Controlled Regioselectivity in the Reductive Cleavage of p-Methoxybenzylidene Acetals
The regioselective ring opening of pyranosidic 4,6-p-methoxybenzylidene acetals with BH(3)/Bu(2)BOTf in THF can be tuned by adjusting the reaction temperature and reagent concentrations. Reductive cleavage at 0 °C resulted in the exclusive formation of 4-O-p-methoxybenzyl (PMB) ethers, whereas react...
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| Main Authors: | , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2004
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1851890/ https://ncbi.nlm.nih.gov/pubmed/15471470 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo048999m |
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