Improvement of the C-glycosylation Step for the Synthesis of Remdesivir
Organic Process Research & Development
; 24(9):1772-1777, 2020.
Article
in English
| Web of Science | ID: covidwho-880187
ABSTRACT
The bulk supply of the antiviral C-nucleoside analogue remdesivir is largely hampered by a low-yielding Cglycosylation step in which the base is coupled to the pentose unit. Here, we disclose a significantly improved methodology for this critical transformation. By utilizing diisopropylamine as a cost-effective additive, the addition reaction furnishes an optimal yield of 75% of the desired ribofuranoside adduct, representing the highest yield obtained thus far for this key step. The method proved suitable for hectogram scale synthesis without column chromatographic operations.
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Collection:
Databases of international organizations
Database:
Web of Science
Language:
English
Journal:
Organic Process Research & Development
Year:
2020
Document Type:
Article
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