Journal of the American Chemical Society · 2013 · 31 citations · 39 references
PharmacyBiochemistryMedicinal ChemistryCarbohydrate ChemistryGlycobiologyNatural Product BiosynthesisCarbohydrate SynthesisGlycan BiosynthesisGlycosidic Bond FormationGlycosylation PathwaysO-linked GlycosylationC-glycoside SynthesisGlycal ChemistryGlycan SynthesisGlycoconjugate SynthesisGlycoside SynthesisGlycosylation DerivatizationNatural Product Total SynthesisTotal Synthesis-derived Analogues
The first total synthesis of vineomycin B2 (1) has been accomplished. The aglycon segment, a vineomycinone B2 derivative, and the glycon segment, an α-L-acurosyl-L-rhodinose derivative, were prepared via C-glycosylation using an unprotected sugar and powerful chemoselective O-glycosylation using a 2,3-unsaturated sugar, respectively, as the key steps. Furthermore, effective and simultaneous introduction of the two glycon moieties to the aglycon part by concentration-controlled glycosylation led to the total synthesis of 1.
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Total synthesis of the macrolide antibiotic cytovaricin
David A. Evans, Stephen W. Kaldor, Todd K. Jones et al. · Journal of the American Chemical Society · 1990 · 312 citations