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Reduction of Sugar Lactones to Hemiacetals with Lithium Triethylborohydride
Reduction of ribono-1,4-lactones and gulono-1,4-lactone as well as ribono-1,5-lactone and glucono-1,5-lactones with LTBH (1.2 equiv.) in CH(2)Cl(2) at 0 °C for 30 min. provided the corresponding pentose or hexose hemiacetals in high yields. Commonly used in carbohydrate chemistry protecting groups s...
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| Pubblicato in: | Carbohydr Res |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4975962/ https://ncbi.nlm.nih.gov/pubmed/27341397 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.carres.2016.06.002 |
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