Selective 3-O-allylation and 3-O-benzylation of methyl α-d-manno-, α-l-rhamno- and β-l-fuco-pyranoside
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference8 articles.
1. Synthesis and conformation of 2,6-dioxabicyclo[3.1.1]heptanes: 1,3-anhydro-2,4,6-tri-O-benzyl-β-d-galactopyranose
2. An efficient, unambiguous synthesis of methyl 3-O-β-d-galactopyranosyl-β-d-galactopyranoside. Further studies on the specificity of antigalactopyranan monoclonal antibodies
3. A mild procedure for the regiospecific benzylation and allylation of polyhydroxy-compounds via their stannylene derivatives in non-polar solvents
4. Synthetic mucin fragments: methyl 3-O-(2-acetamido-2-deoxy-β-d-glucopyranosyl)-β-d-galactopyranoside and methyl 3-O-(2-acetamido-2-deoxy-3-O-β-d-galactopyranosyl-β-d-glucopyranosyl)-β-d-galactopyranoside
5. Synthesis of β--mannopyranosides and regioselective -alkylation of dibutylstannylene complexes
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