Synthesis and glycosidic coupling reaction of substituted 2,6-dioxabicyco[3.1.1] heptanes: 1,3-anhydro-2-azido-4,6-di-O-benzyl-2-deoxy-β-d-mannopyranose

[1]  W. Liao,et al.  Convergent synthesis of an octasaccharide acceptor corresponding to the reducing terminus of mycobacterial 3-O-methylmannose polysaccharide (MMP) , 1997 .

[2]  P. Jansson,et al.  Structural studies of the O-antigenic polysaccharide from an Aeromonas caviae strain. , 1996, Carbohydrate research.

[3]  Yuguo Du,et al.  Synthesis, conformation and glycosylation reaction of substituted 2,6-dioxabicyclo[3.1.1]heptanes:1,3-anhydro-2,4-di-O-benzyl-α-l-arabinopyranose , 1995 .

[4]  Shunya Takahashi,et al.  Preparation of a Highly Functionalized Cyclopentane Derivative Suitable for the Synthesis of Allosamidin Analogs , 1995 .

[5]  J. Banoub,et al.  Synthesis of oligosaccharides of 2-amino-2-deoxy sugars , 1992 .

[6]  D. Lu,et al.  Synthesis and conformational analysis of substituted 2,6-dioxabicyclo[3.1.1]heptanes: 1,3-anhydro-2,4-di-O-benzyl-6-deoxy-β-d-glucopyranose by 1H-NMR spectroscopy and molecular mechanics calculation , 1992 .

[7]  F. Kong,et al.  Synthesis and Conformation of Substituted 2,6-Dioxabiocyclo[3.1.1]heptanes: 1, 3-Anhydro-2, 4-di-O-benzyl-β-D-fucopyranose , 1992 .

[8]  D. Lu,et al.  Synthesis and Conformation of Substituted 2,6-Dioxabicyclo[3.1.1]Heptanes: 1,3-Anhydro-6-Azido-2,4-Di-O-Benzyl-6-Deoxy- And 1,3-Anhydro-6-Azido-2,4-Di-O-(P-Bromobenzyl)-6-Deoxy-β-D-Mannopyranose , 1991 .

[9]  D. Lu,et al.  Synthesis and conformation of 2,6-dioxabicyclo[3.1.1]heptanes: 1,3-anhydro-2,4,6-tri-O-benzyl-β-d-galactopyranose , 1990 .

[10]  B. Su,et al.  Synthesis and conformational analysis of substituted 2,6-dioxabicyclo[3.1.1]heptanes: 1,3-anhydro-2,4-di-O-benzyl- and -2,4-di-O-(p-bromobenzyl)-β-l-rhamnopyranose , 1987 .

[11]  C. Schuerch,et al.  Improved synthesis of substituted 2,6-dioxabicyclo[3.1.1]heptanes: 1,3-anhydro-2,4,6-tri-O-benzyl-2,4,6-tri-O-p-bromobenzyl- and -2,4,6-tri-O-p-methylbenzyl-β-d-glucopyranose , 1984 .

[12]  C. Schuerch,et al.  Improved synthesis of substituted 2,6-dioxabicyclo[3.1.1]heptanes: 1,3-anhydro-2,4,6-tri-O-benzyl- and 1,3-anhydro-2,4,6-tri-O-p-bromobenzyl-β-d-mannopyranose , 1983 .

[13]  A. Varma,et al.  Correction. Synthesis of Substituted 2,6-Dioxabicyclo[3.1.1]heptanes. 1,3-Anhydro-2,4,6-tri-O-benzyl- and 1,3-Anhydro-2,4,6-tri-O-(p-bromobenzyl)-β-D-mannopyranose. , 1981 .

[14]  Hiroshi Ito,et al.  Synthesis of a substituted 2,6-dioxabicyclo[3.1.1]heptane,1,3-anhydro-2,4,6-tri-O-benzyl-β-d-glucopyranose , 1980 .

[15]  M. Hamberg,et al.  Thromboxanes: a new group of biologically active compounds derived from prostaglandin endoperoxides. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[16]  I. Dyong,et al.  Partiell benzylierte Kohlenhydrate, 2. Synthese aller Methyl‐mono‐, Methyl‐di‐ und Methyl‐tri‐O‐benzyl‐α‐D‐glucopyranoside. , 1975 .

[17]  Nasir-ud-din,et al.  Synthesis of the 3- and 4-methyl, 3,4-dimethyl, and 3,4,6-trimethyl ethers of methyl 2-acetamido-2-deoxy-alpha-D-mannopyranoside. , 1973, Carbohydrate research.