616201-13-9Relevant articles and documents
Rapid assembly of the doubly-branched pentasaccharide domain of the immunoadjuvant jujuboside A: Via convergent B(C6F5)3-catalyzed glycosylation of sterically-hindered precursors
Karimov, Rashad R.,Tan, Derek S.,Gin, David Y.
supporting information, p. 5838 - 5841 (2017/07/11)
A convergent synthesis of the complex, doubly-branched pentasaccharide domain of the natural-product immunoadjuvant jujuboside A is described. The key step is a sterically-hindered glycosylation reaction between a branched trisaccharide trichloroacetimida
The first total synthesis of calabricoside A
Du, Yuguo,Wei, Guohua,Linhardt, Robert J.
, p. 6887 - 6890 (2007/10/03)
Quercetin 3-O-[α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranoside] -7-O-β-D-glucopyranoside (calabricoside A), a new flavonol triglycoside isolated from the aerial parts of Putoria calabrica showing strong radical scavenging activity, was synthesized through