Cipolla, Laura published the artcileGlycosyl sulfates as glycosyl donors, Quality Control of 87905-98-4, the main research area is glycosyl sulfate glycosidation; glycoside preparation glycosyl sulfate; disaccharide preparation glycosyl sulfate.
2,3,4,6-Tetra-O-benzyl-D-glucopyranose was treated with SO3.NMe3 complex to give 2,3,4,6-tetra-O-benzyl-D-glucopyranosyl sulfate trimethylamine salt (α:β = 3:1), which when reacted with various acceptors promoted by Lewis acids gave glycosides and disaccharides as α,β mixtures For example, coupling 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl sulfate with 2,3,4,6-tetra-O-α-D-glucopyranose gave trehaloses in 96% overall yield (β,α:α,α:β,β = 8:4:3).
Tetrahedron Letters published new progress about Glycosylation. 87905-98-4 belongs to class alcohols-buliding-blocks, name is Benzyl (5-hydroxypentyl)carbamate, and the molecular formula is C13H19NO3, Quality Control of 87905-98-4.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts