Synthesis of 4” manipulated Lewis X trisaccharide analogues

scientific article published on July 23, 2012

Synthesis of 4” manipulated Lewis X trisaccharide analogues is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.3762/BJOC.8.126
P953full work available online athttp://www.beilstein-journals.org/bjoc/content/8/1/126
https://europepmc.org/articles/PMC3458731
https://europepmc.org/articles/PMC3458731?pdf=render
https://www.beilstein-journals.org/bjoc/articles/8/126
https://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-8-126.pdf
P932PMC publication ID3458731
P698PubMed publication ID23019441
P5875ResearchGate publication ID231225572

P2093author name stringFrance-Isabelle Auzanneau
Christopher J. Moore
P2860cites workSynthesis of spacer-equipped phosphorylated di-, tri- and tetrasaccharide fragments of the O-specific polysaccharide of Vibrio cholerae O139Q28196938
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Why are the hydroxy groups of partially protected N-acetylglucosamine derivatives such poor glycosyl acceptors, and what can be done about it? A comparative study of the reactivity of N-acetyl-, N-phthalimido-, and 2-azido-2-deoxy-glucosamine derivaQ33423429
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Localization and alteration of mono-, di-, and trifucosyl alpha 1----3 type 2 chain structures during human embryogenesis and in human cancerQ36349361
Lewis x is highly expressed in normal tissues: a comparative immunohistochemical study and literature revisionQ36868517
Molecular Recognition of Sialyl Lewisxand Related Saccharides by Two LectinsQ38295466
O-antigen biotin conjugates preparation and use in direct competitive enzyme immunoassaysQ38339221
Synthesis of a BSA-Le(x) glycoconjugate and recognition of Le(x) analogues by the anti-Le(x) monoclonal antibody SH1: the identification of a non-cross reactive analogueQ38340863
Synthesis of type 2 human blood-group antigenic determinants. The H, X, and Y haptens and variations of the H type 2 determinant as probes for the combining site of the lectin I of Ulex europaeusQ38355170
Synthesis of Lewis X trisaccharide analogues in which glucose and rhamnose replace N-acetylglucosamine and fucose, respectivelyQ38355359
Total synthesis of X hapten, III3 Fuc alpha-nLc4 Cer.Q42067267
Synthesis of a tri- and a hepta-saccharide which contain alpha-L-fucopyranosyl groups and are part of the complex type of carbohydrate moiety of glycoproteinsQ42228789
Synthesis of Le(a)Le(x) oligosaccharide fragments and efficient one-step deprotectionQ43088537
How the substituent at O-3 of N-acetylglucosamine impacts glycosylation at O-4: a comparative studyQ43265662
A highly efficient synthetic strategy for polymeric support synthesis of Le(x), Le(y), and H-type 2 oligosaccharidesQ43669118
Synthesis of building blocks of human milk oligosaccharides. Fucosylated derivatives of the lacto- and neolacto-series.Q44120700
Complex oligosaccharide investigations: synthesis of an octasaccharide incorporating the dimeric Le(x) structure of PSGL-1.Q44380187
Profiles of Lewisx-containing glycoproteins and glycolipids in sera of patients with adenocarcinomaQ44387332
Assembly of a series of malarial glycosylphosphatidylinositol anchor oligosaccharidesQ45281664
Application and limitations of the methyl imidate protection strategy of N-acetylglucosamine for glycosylations at O-4: synthesis of Lewis A and Lewis X trisaccharide analoguesQ46359622
Convenient temporary methyl imidate protection of N-acetylglucosamine and glycosylation at O-4.Q46393285
Synthesis of Lewis X and three Lewis X trisaccharide analogues in which glucose and rhamnose replace N-acetylglucosamine and fucose, respectivelyQ46604814
The amide group in N-acetylglucosamine glycosyl acceptors affects glycosylation outcomeQ46623545
Unusual conformational behavior of trisaccharides containing N-acetylglucosamineQ46768404
Differential expression of Lewis(x) and sialyl-Lewis(x) antigens in fetal human neural cells in cultureQ48169369
Location and distribution of difucoganglioside (VI3NeuAcV3III3Fuc2nLc6) in normal and tumor tissues defined by its monoclonal antibody FH6.Q53798317
Computer simulation of histo-blood group oligosaccharides: energy maps of all constituting disaccharides and potential energy surfaces of 14 ABH and Lewis carbohydrate antigensQ56084985
A Novel and Efficient Synthesis of a Dimeric LexOligosaccharide on Polymeric SupportQ57242579
Crystal and molecular structure of a histo-blood group antigen involved in cell adhesion: the Lewis x trisaccharideQ57242974
Solution structure of the Lewis x oligosaccharide determined by NMR spectroscopy and molecular dynamics simulationsQ67519118
Synthesis of oligosaccharides containing the X-antigenic trisaccharide (alpha-L-Fucp-(1----3)-[beta-D-Galp-(1----4)]-beta-D-GlcpNAc) at their nonreducing endsQ68010545
Lewisx- and sialylated Lewisx-related antigen expression in human malignant and nonmalignant colonic tissuesQ68871716
Mosaicism in the expression of tumor-associated carbohydrate antigens in human colonic and gastric cancersQ69506209
Oligosaccharides of human milk. II. Isolation and characterization of a new pentasaccharide, lacto-N-fucopentaose 3Q71230172
A Sphingolipid Having a Novel Type of Ceramide and Lacto-N-Fucopentaose IIIQ71760939
Total synthesis of sulfated Le(x) pentaosyl ceramideQ72368601
Novel fucolipids accumulating in human adenocarcinoma. II. Selective isolation of hybridoma antibodies that differentially recognize mono-, di-, and trifucosylated type 2 chainQ72728094
Active-latent glycosylation strategy toward Lewis X pentasaccharide in a form suitable for neoglycoconjugate synthesesQ73068061
Glycosylation of N-acetylglucosamine: imidate formation and unexpected conformationQ73685611
Selection of tumor antigens as targets for immune attack using immunohistochemistry: II. Blood group-related antigensQ73798453
Synthesis of N-acetylglucosamine containing Lewis A and Lewis X building blocks based on N-tetrachlorophthaloyl protection--synthesis of Lewis X pentasaccharideQ77534570
Stereospecific ester activation in nitrite-mediated carbohydrate epimerizationQ83111824
Syntheses and NMR characterizations of epimeric 4-deoxy-4-fluoro carbohydratesQ84927536
An efficient synthesis of the Lewis X (Lex) antigen familyQ127237288
P407language of work or nameEnglishQ1860
P921main subjectoligosaccharide biosynthetic processQ21109511
alpha-L-Fucp-(1->3)-[beta-D-Galp4Cl-(1->4)]-beta-D-GlcpNAc-OMeQ27146753
alpha-L-Fucp-(1->3)-[beta-D-Galp4F-(1->4)]-beta-D-GlcpNAc-OMeQ27146754
4-chloro-4-deoxygalactoseQ106490025
P304page(s)1134-1143
P577publication date2012-07-23
P1433published inBeilstein Journal of Organic ChemistryQ2894008
P1476titleSynthesis of 4" manipulated Lewis X trisaccharide analogues
Synthesis of 4” manipulated Lewis X trisaccharide analogues
P478volume8

Reverse relations

cites work (P2860)
Q42174680Multivalent glycosystems for nanoscience
Q99591021Recognition of Dimeric Lewis X by Anti-Dimeric Lex Antibody SH2
Q91010790Recognition of Lewis X by Anti-Lex Monoclonal Antibody IG5F6
Q48262784Synthesis of Protected 3-Deoxy-3-fluoro- and 4-Deoxy-4-fluoro-d-galactopyranosides from Levoglucosan.
Q64277570Synthesis of carbohydrate building blocks via regioselective uniform protection/deprotection strategies
Q42709282Understanding the recognition of Lewis X by anti-Le(x) monoclonal antibodies

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