6027-42-5Relevant articles and documents
Larger laboratory scale synthesis of 5-methyluridine and formal synthesis of its L-enantiomer
Thiesen, Luciano J. Hoeltgebaum,Cabral, Nadia,Joselice E Silva, Maria,Bezerra, Gilson,Doboszewski, Bogdan
, p. 249 - 264 (2017/06/19)
A larger laboratory scale synthesis (>60 g per run) of 5-methyluridine is presented. The critical intermediate 1,2-O-isopropylidene-α-D-ribofuranose was prepared from very cheap D-glucose via D-allose. Its L-enantiomer was obtained from L-arabinose via L-glucose, and also from L-xylose. {figure presented}.
Synthesis of daunosamine
Grethe,Mitt,Williams,Uskokovic
, p. 5309 - 5315 (2007/10/02)
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