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Synthesis of N-methyl-d-ribopyranuronamide nucleosides
The synthesis of N-methyl-d-ribopyranuronamide nucleosides is described. The key route is the rearrangement of a 1,2-O-isopropylidene protected furanose sugar with a carboxamide function in the 4-position to a ribopyranuronamide ring. The Lewis acid catalyzed condensation of adenine and thymine nucl...
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| Publicado no: | Tetrahedron |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier Ltd.
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7126205/ https://ncbi.nlm.nih.gov/pubmed/32287418 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tet.2008.08.027 |
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