61236-82-6Relevant articles and documents
Total Synthesis of Alvaradoins e and F, Uveoside, and 10-epi-Uveoside
Ng, Kevin,Shaktah, Ryan,Vardanyan, Laura,Minehan, Thomas G.
, p. 9175 - 9178 (2019)
Concise total syntheses of the anthracenone C-glycosides alvaradoins E and F, uveoside, and 10-epi-uveoside (1-4) have been accomplished from chrysophanic acid 8 and bromosugar 9. Key steps in the syntheses include the DBU-induced coupling of 8 and 9 to p
Synthesis of cis-(1 → 3)-glycosides of allyl 2-acetamido-4,6-O- benzylidene-2-deoxy-α-D-glucopyranoside
Madaj, Janusz,Jankowska, Magdalena,Wisniewski, Andrzej
, p. 1293 - 1300 (2007/10/03)
Syntheses of allyl 2,3,4-tri-O-benzyl-α-D-gluco- and D-galactopyranosyluronate-(1→3)-2-acetamido-4,6-O-benzylidene-2-deoxy- α-D-glucopyranoside via oxidation of the hydroxymethyl group of allyl 2,3,4-tri-O-benzyl-α-D-gluco- and D-galactopyranosyl-(1→3)-2-
Synthesis of hexasaccharide fragments of pectin
Clausen, Mads H.,Madsen, Robert
, p. 3821 - 3832 (2007/10/03)
Abstract: Short syntheses of partially methyl-esterified hexagalacturonates 1-5 are described as part of the development of strategies for the preparation of larger pectic oligosaccharides. The methodology is based on the repeated coupling of galactose mo
Synthesis of the pentasaccharide chain of the Forsman antigen
Paulsen,Buensch
, p. 143 - 167 (2007/10/02)
The pentasaccharide chain of the Forssman antigen, O-(2-acetamido-2-deoxy-alpha-D-galactopyranosyl)-(1 leads to 3)-O-(2-acetamido-2-deoxy-beta-D-galactopyranosyl)-(1 leads to 3)-O-alpha-D-galactopyranosyl-(1 leads to 4)-O-beta-D-galactopyranosyl-(1 leads
Bausteine von Oligosacchariden, XXIX. Synthese des Trisaccharids aus N-Acetylglucosamin, Galactose und Rhamnose einer O-determinanten Kette von Escherichia coli. Abhaengigkeit der Stereoselektivitaet der α-Glycosidsynthese von der Reaktivitaet des Pyranos
Paulsen, Hans,Lockhoff, Oswald
, p. 3079 - 3101 (2007/10/02)
The mercury salt catalysed reaction of substituted α-D-galactosyl halides with the reactive 4-OH groups of the rhamnosides 18 and 19 were studied.The order of reactivity of the halides increases with the following substituents: O-acetyl O-glucosyl O-b