138857-85-9Relevant academic research and scientific papers
Unusual reactivity of pyruvated glycosyl donors during construction of rhizobial exopolysaccharide fragments
Ziegler, Thomas,Eckhardt, Elisabeth
, p. 534 - 540 (2007/10/03)
Two pyruvated galactosyl donors, 2,3-di-O-benzoyl-4,6-0-[1-(R)-methoxycarbonyl(ethylidene)]-α-D- galactopyranosyl chloride (6) and trichloroacetimidate 13, were coupled to position 3 of suitably protected mono and disaccharide benzyl glucoside acceptors. For both donors, an unusual high content of the α-(1→3)-linked products was obtained. The corresponding β-(1→3)-linked di- and trisaccharides are related to exopolysaccharides of Rhizobium leguminosarum.
Lewis Acid-Catalysed Anomerisation and Rearrangement of Alkyl D-Glycopyranosides During Acetalisation with Methyl Pyruvate: How to Utilise it for the Preparation of 1-(Carboxyethylidene)glycopyranosyl Donors
Ziegler, Thomas,Eckhardt, Elisabeth,Herold, Gerhard
, p. 441 - 452 (2007/10/02)
The preparation of 4,6-O-(1-methoxycarbonylethylidene)-D-glycopyranosides 5 starting from 2,3-di-O-benzoyl-D-glycopyranosides 1 and their 4,6-bis-O-trimethylsilyl ethers 2 using methyl 2,2-bis(phenylthio)propionate (4) and methyl pyruvate (3), respectivel
