Stereoselective Total Synthesis of 1,4-Dideoxy-1,4-imino-L-ribitol by an Intramolecular Ring Opening of Epoxide with a Tethered Amide
Stereoselective total synthesis of 1,4-dideoxy-1,4-imino-L-ribitol has been accomplished from D -glucose. The key step involved in this synthesis is the regioselective ring-opening of the epoxide with a tethered amido group to give the N -tosyl-3,6-dideoxy-3,6-imino-1,2- O -isopropylidene-α-D-glucof...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publishing
2018-08-01
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| coleção: | Natural Product Communications |
| Acesso em linha: | https://doi.org/10.1177/1934578X1801300821 |
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