Concepedia

Synthesis of methyl 3--[3--(2,3,4-tri--methyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl]-α-L-rhamnopyranoside : The outer trisaccharide unit of a unique glycopeptidolipid

Mukund K. Gurjar, A. S. Mainkar

Tetrahedron · 1992 · 17 citations · 11 references

Concepts

Methyl 3Natural Product SynthesisBioorganic ChemistryBiochemistryNatural SciencesMedicineGlycobiologyStereoselective SynthesisPharmacologyUnique GlycopeptidolipidCarbohydrate-protein InteractionBiomolecular EngineeringGlycosylation

References

11

New Methods for the Synthesis of Glycosides and Oligosaccharides—Are There Alternatives to the Koenigs‐Knorr Method? [New Synthetic Methods (56)]

Richard R. Schmidt · Angewandte Chemie International Edition in English · 1986 · 1.4K citations

Proteinlipid Interaction, Bioorganic Chemistry, Koenigs‐knorr Method +20

Regioselective manipulation of hydroxyl groups via organotin derivatives

Stephen Hanessian · Tetrahedron · 1985 · 623 citations

Engineering, Organic Chemistry, Stereoselective Synthesis +3

Selective deacetylation of anomeric sugar acetates with tin alkoxides

Abraham Nudelman, J. Herzig, Hugo E. Gottlieb et al. · Carbohydrate Research · 1987 · 76 citations

Selective Deacetylation, Organic Chemistry, Stereoselective Synthesis +3

Synthesis of partially protected benzyl and methyl α-l-rhamnopyranosides by the phase-transfer technique

Vince Pozsgay · Carbohydrate Research · 1979 · 65 citations

Phase-transfer Technique, Organic Chemistry, Chemistry +3

Synthetic oligosaccharides related to Group B streptococcal polysaccharides. The rhamnotriose moiety of the common antigen

Vince Pozsgay, Jean‐Robert Brisson, Harold J. Jennings · Canadian Journal of Chemistry · 1987 · 45 citations

Bioorganic Chemistry, Common Antigen Polysaccharide, Glycobiology +16