| Literature DB >> 26612347 |
Ziyang Zhang1, Takehiro Fukuzaki1, Andrew G Myers2.
Abstract
D-Desosamine is synthesized in 4 steps from methyl vinyl ketone and sodium nitrite. The key step in this chromatography-free synthesis is the coupling of (R)-4-nitro-2-butanol and glyoxal (trimeric form) mediated by cesium carbonate, which affords in crystalline form 3-nitro-3,4,6-trideoxy-α-D-glucose, a nitro sugar stereochemically homologous to D-desosamine. This strategy has enabled the syntheses of an array of analogous 3-nitro sugars. In each case the 3-nitro sugars are obtained in pure form by crystallization.Entities:
Keywords: 3-amino sugars; Henry reaction; desosamine; macrolide antibiotics; γ-nitro alcohols
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Year: 2015 PMID: 26612347 DOI: 10.1002/anie.201507357
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336