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Evolution of the Synthesis of Remdesivir. Classical Approaches and Most Recent Advances
Didier F Vargas1, Enrique L Larghi1, Teodoro S Kaufman1
1Instituto de Química Rosario (IQUIR, CONICET-UNR) and National University of Rosario (UNR), Suipacha 531, 2000 Rosario, Argentina.
Abstract:
The broad-spectrum antiviral Remdesivir, a monophosphate nucleoside analogue prodrug (ProTide), was repurposed. In May 2020, it received emergency approval by the FDA, being the first drug approved to fight the new coronavirus (COVID-19) disease which targets the virus directly. The main synthetic strategies toward Remdesivir, and their relevant modifications, are presented and discussed, to provide a panoramic view of the state-of-the-art and the more important advances in this field. Recent progress, proposed improvements, and uses of novel technologies for the synthetic sequence are also detailed.
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