Highly alpha-selective sialyl phosphate donors for efficient preparation of natural sialosides.
about
Carbohydrate-based vaccines with a glycolipid adjuvant for breast cancerMethodology development and physical organic chemistry: a powerful combination for the advancement of glycochemistry.Synthesis and immunological study of α-2,9-oligosialic acid conjugates as anti-group C meningitis vaccines.Toward automated oligosaccharide synthesis.Synthesis and labeling of α-(2,9)-trisialic acid with cyanine dyes for imaging of glycan-binding receptors on living cells.One-pot synthesis of N-acetyl- and N-glycolylneuraminic acid capped trisaccharides and evaluation of their influenza A(H1 N1) inhibition.Probing the influence of protecting groups on the anomeric equilibrium in sialic acid glycosides with the persistent radical effectExploration of the Oxazolidinthione Protecting System for the Synthesis of Sialic Acid Glycosides.Stereoselective C-glycoside formation with 2-O-benzyl-4,6-O-benzylidene protected 3-deoxy gluco- and mannopyranoside donors: comparison with O-glycoside formation.Dissecting the influence of oxazolidinones and cyclic carbonates in sialic acid chemistry.Probing the influence of a 4,6-O-acetal on the reactivity of galactopyranosyl donors: verification of the disarming influence of the trans-gauche conformation of C5-C6 bonds.Influence of side chain conformation and configuration on glycosyl donor reactivity and selectivity as illustrated by sialic acid donors epimeric at the 7-position.Influence of protecting groups on the anomeric equilibrium; case of the 4,6-O-benzylidene acetal in the mannopyranose seriesAutomated solid-phase synthesis of oligosaccharides containing sialic acids.Oxidative Deamination of N-Acetyl Neuraminic Acid: Substituent Effects and Mechanism.A minimalist approach to stereoselective glycosylation with unprotected donors.Chemical diversification of sialic acid glycosides by stereospecific, chemoselective deamination.Chemical Synthesis of the Repeating Unit of Type V Group B Streptococcus Capsular Polysaccharide.The isothiocyanato moiety: an ideal protecting group for the stereoselective synthesis of sialic acid glycosides and subsequent diversification.Highly efficient α-C-sialylation promoted by (p-Tol)2SO/Tf2O with N-acetyl-5-N,4-O-oxazolidione protected thiosialoside as donor.Synthesis of Neisseria meningitidis serogroup W135 capsular oligosaccharides for immunogenicity comparison and vaccine development.Total Biosynthesis of Legionaminic Acid, a Bacterial Sialic Acid Analogue.Synthesis of an S-Linked α(2→8) GD3 Antigen and Evaluation of the Immunogenicity of Its Glycoconjugate.The α-Glycosidation of Partially Unprotected N-Acetyl and N-Glycolyl Sialyl Donors in the Absence of a Nitrile Solvent Effect.Stereoselective Synthesis of 5-epi-α-Sialosides Related to the Pseudaminic Acid Glycosides. Reassessment of the Stereoselectivity of the 5-Azido-5-deacetamidosialyl Thioglycosides and Use of Triflate as Nucleophile in the Zbiral Deamination of SialiABO Antigens Active Tri- and Disaccharides Microarray to Evaluate C-type Lectin Receptor Binding Preferences.
P2860
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P2860
Highly alpha-selective sialyl phosphate donors for efficient preparation of natural sialosides.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
Highly alpha-selective sialyl ...... aration of natural sialosides.
@en
Highly alpha-selective sialyl ...... aration of natural sialosides.
@nl
type
label
Highly alpha-selective sialyl ...... aration of natural sialosides.
@en
Highly alpha-selective sialyl ...... aration of natural sialosides.
@nl
prefLabel
Highly alpha-selective sialyl ...... aration of natural sialosides.
@en
Highly alpha-selective sialyl ...... aration of natural sialosides.
@nl
P2093
P356
P1476
Highly alpha-selective sialyl ...... aration of natural sialosides.
@en
P2093
Che-Hsiung Hsu
Chi-Huey Wong
Chien-Tai Ren
Chung-Yi Wu
Jeng-Liang Han
Kuo-Ching Chu
Yih-Shyan Lin
Yu-Shiang Peng
P304
P356
10.1002/CHEM.200903035
P407
P577
2010-02-01T00:00:00Z