This search combines search strings from the content search (i.e. "Full Text", "Author", "Title", "Abstract", or "Keywords") with "Article Type" and "Publication Date Range" using the AND operator.
Beilstein J. Org. Chem. 2012, 8, 413–420, doi:10.3762/bjoc.8.46
Graphical Abstract
Figure 1: Monobenzylated methyl α- and β-D-gluco- and galactopyranoside acceptors 1–6.
Figure 2: Benzylated glycopyranosyl halide donors 7–9.
Scheme 1: Synthesis of monobenzylated glucopyranosyl acceptors 1–4. Reagents and conditions: (a) Benzaldehyde...
Scheme 2: Synthesis of 3-O-monobenzylated gluco- und galactopyranosyl acceptors 5 and 6. Reagents and conditi...
Scheme 3: Synthesis of 2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl chloride (8) and 2,3,4,6-tetra-O-benzyl-α-...
Beilstein J. Org. Chem. 2010, 6, No. 18, doi:10.3762/bjoc.6.18
Figure 1: Structures of pentasaccharides 1 and 2.
Scheme 1: Preparation of pentasaccharide 8. 1) MeOH, acidic ion exchange resin; 2) Ac2O, pyridine; 3) 80% HOA...
Scheme 2: Preparation of pentasaccharide 14. 1) MeOH, acidic ion exchange resin; 2) Ac2O, pyridine; 3) 80% HO...
Figure 2: Roman numbering of saccharide units in all pentasaccharides for NMR assignment.