Preactivation-based chemoselective glycosylations: A powerful strategy for oligosaccharide assembly

• Weizhun Yang,
• Bo Yang,
• Sherif Ramadan and
• Xuefei Huang

Beilstein J. Org. Chem. 2017, 13, 2094–2114, doi:10.3762/bjoc.13.207

• ]. The displacement of the anomeric hydroxy group of a glycosyl hemiacetal by an acceptor for dehydrative glycosylation is an interesting alternative as glycosyl hemiacetals are often undesired side products in glycosylation reactions due to the competitive reaction with trace amounts of water present in

• glycosyl hemiacetal 33 with one of its hydroxy groups free available as the acceptor producing disaccharide 34. The regioselectivity is presumably due to the higher nucleophilicity of the alkyl hydroxy group than that of the hemiacetal hydroxy group. This process can be repeated for chain elongation

• acid synthesis. With continuous development, the preactivation strategy will achieve wider applications in complex carbohydrate synthesis. Representative structures of products formed by the preactivation-based dehydrative glycosylation of glycosyl hemiacetal. Retrosynthetic analysis of pentasaccharide

Synthesis of D-fructose-derived spirocyclic 2-substituted-2-oxazoline ribosides

• Madhuri Vangala and
• Ganesh P. Shinde

Beilstein J. Org. Chem. 2015, 11, 2289–2296, doi:10.3762/bjoc.11.249

• with nitrile solvents, providing a transient α,β-glycosyl nitrilium species that could produce an oxazolinium intermediate through the participation of the vicinal oxygen atom. In 1981, Pavia and co-workers proposed the formation of uncharacterized oxazolinium from glycosyl hemiacetal in acetonitrile

Appel-reagent-mediated transformation of glycosyl hemiacetal derivatives into thioglycosides and glycosyl thiols

• Tamashree Ghosh,
• Abhishek Santra and
• Anup Kumar Misra

Beilstein J. Org. Chem. 2013, 9, 974–982, doi:10.3762/bjoc.9.112

• Tamashree Ghosh Abhishek Santra Anup Kumar Misra Bose Institute, Division of Molecular Medicine, P-1/12, C.I.T. Scheme VII-M, Kolkata-700054, India, Fax: 91-33-2355 3886 10.3762/bjoc.9.112 Abstract A series of glycosyl hemiacetal derivatives have been transformed into thioglycosides and glycosyl

• carbonotrithioate. The reaction conditions are reasonably simple and yields were very good. Keywords: Appel reagent; carbon tetrabromide; glycosyl hemiacetal; glycosyl thiol; thioglycoside; triphenylphosphine; Introduction Thioglycosides (1-thiosugar) are widely used glycosyl donors in glycosylation reactions [1

• various thiooligosaccharides, glycoproteins and glycolipids [28][29][30][31][32]. The anomeric configurations of glycosyl thiols mostly remain unaffected in comparison to the glycosyl hemiacetal derivatives during their synthetic transformations [4]. Glycosyl thiol derivatives act as precursors for the