Sheppard, Daniel J. published the artcileComparison of disaccharide donors for heparan sulfate synthesis: uronic acids vs. their pyranose equivalents, HPLC of Formula: 4972-31-0, the publication is Organic & Biomolecular Chemistry (2020), 18(25), 4728-4733, database is CAplus and MEDLINE.
Late oxidation of hexose based building blocks or the use of uronic acid containing building blocks are two complementary strategies in the synthesis of glycosaminoglycans. Here we report the synthesis and evaluation of various disaccharide donors-uronic acids and their pyranose equivalent-for the synthesis of heparan sulfate, using an established protective group strategy. Hexose based “imidate” type donors perform well in the studied glycosylation, while their corresponding uronate esters fall short; a uronate ester thioglycoside performs equal to, if not better than, a hexose thioglycoside equivalent
Organic & Biomolecular Chemistry published new progress about 4972-31-0. 4972-31-0 belongs to piperidines, auxiliary class Piperidine,Benzene, name is 1-(Phenylsulfinyl)piperidine, and the molecular formula is C4H4N2O2, HPLC of Formula: 4972-31-0.
Referemce:
https://en.wikipedia.org/wiki/Piperidine,
Piperidine | C5H11N – PubChem