Park, Simon S.; Gervay-Hague, Jacquelyn published the artcile< Step-economy synthesis of β-steryl sialosides using a sialyl iodide donor>, Reference of 4064-06-6, the main research area is crystal structure conformation sialic acid preparation steroid glycoside; steryl sialoside synthesis sialyl iodide neuraminic acid glycosylation.
Steryl glycosides are prevalent in nature and have unique biol. activities dictated by sterol structure, sugar composition, and the stereochem. attachment of the aglycon. A single configurational switch can have profound biol. consequences meriting the systematic study of structure and function relationships. Steryl congeners of N-acetyl neuraminic acid (NANA) impact neurobiol. processes and may also mediate host/microbe interactions. In order to study these processes, a platform for the synthesis of β-steryl sialosides has been established. Promoter-free glycosidations using a novel α-linked sialyl iodide donor efficiently provide unique amphiphilic sialoglycoconjugates for examining bioactivities in various systems.
Journal of Antibiotics published new progress about Amphiphiles. 4064-06-6 belongs to class alcohols-buliding-blocks, and the molecular formula is C12H20O6, Reference of 4064-06-6.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts