[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Mong et al., 2003 - Google Patents

Reactivity-based one-pot total synthesis of fucose GM1 oligosaccharide: A sialylated antigenic epitope of small-cell lung cancer

Mong et al., 2003

View HTML @Full View
Document ID
16397737025052579522
Author
Mong T
Lee H
Durón S
Wong C
Publication year
Publication venue
Proceedings of the National Academy of Sciences

External Links

Snippet

The total synthesis of the sialic acid-containing antigenic epitope fucose GM1 (Fuc-GM1) by an improved reactivity-based one-pot synthetic strategy is reported. Based on a thioglycoside reactivity database, three saccharide building blocks, 3, 4, and 5, were …
Continue reading at www.pnas.org (HTML) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/02Acyclic radicals, not substituted by cyclic structures
    • C07H15/04Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
    • C07H15/10Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical containing unsaturated carbon-to-carbon bonds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/18Acyclic radicals, substituted by carbocyclic rings

Similar Documents

Publication Publication Date Title
Mong et al. Reactivity-based one-pot total synthesis of fucose GM1 oligosaccharide: A sialylated antigenic epitope of small-cell lung cancer
Hahm et al. Automated assembly of oligosaccharides containing multiple cis-glycosidic linkages
Kulkarni et al. “One-pot” protection, glycosylation, and protection–glycosylation strategies of carbohydrates
Hagen et al. Synthesis of the Staphylococcus aureus strain M capsular polysaccharide repeating unit
Gadikota et al. Stereocontrolled synthesis of 2, 3-anhydro-β-D-lyxofuranosyl glycosides
Ngoje et al. Stereocontrolled synthesis of the equatorial glycosides of 3-deoxy-D-manno-oct-2-ulosonic acid: Role of side chain conformation
van Well et al. Iodine Promoted Glycosylation with Glycosyl Iodides: α‐Glycoside Synthesis
Li et al. General strategy for the synthesis of rare sugars via Ru (II)-catalyzed and Boron-mediated selective epimerization of 1, 2-trans-diols to 1, 2-cis-diols
Crich et al. Synthesis of the antigenic tetrasaccharide side chain from the major glycoprotein of Bacillus anthracis exosporium
Krog-Jensen et al. Stereospecific synthesis of β-D-fructofuranosides using thioglycoside donors and internal aglycon delivery
Hevey et al. A scalable approach to obtaining orthogonally protected β-d-idopyranosides
Crich et al. Synthesis and Stereoselective Glycosylation of D-and L-glycero-β-D-manno-Heptopyranoses
Boltje et al. Versatile set of orthogonal protecting groups for the preparation of highly branched oligosaccharides
Kulkarni et al. Two-step synthesis of the immunogenic bacterial glycolipid BbGL1
Gadikota et al. Synthesis of oligosaccharide fragments of mannosylated lipoarabinomannan appropriately functionalized for neoglycoconjugate preparation
Zhang et al. Stereoselective gold (I)-catalyzed approach to the synthesis of complex α-glycosyl phosphosaccharides
Sabbavarapu et al. Automated glycan assembly of oligogalactofuranosides reveals the influence of protecting groups on oligosaccharide stability
Dhurandhare et al. Synthesis of D-galactosamine and D-allosamine derivatives via a microwave-assisted preparation of 1, 6-anhydroglucosamine
Hsieh et al. Two‐step functionalization of oligosaccharides using glycosyl iodide and trimethylene oxide and its applications to multivalent glycoconjugates
Nitz et al. Efficient Synthesis of 3, 6-Dideoxy-β-d-a rabino-hexopyranosyl-Terminated LacdiNac Glycan Chains of the Trichinella s piralis Parasite
Xu et al. Stereoselective synthesis of the trisaccharide moiety of ganglioside HLG-2
Wei et al. Silver triflate. A mild alternative catalyst for glycosylation conditions using trichloroacetimidates as glycosyl donors
Neralkar et al. Nucleofuge Generating Glycosidations by the Remote Activation of Hydroxybenzotriazolyl Glycosides
Wang et al. Highly Regio-and Stereoselective Synthesis of Bioactive Oligosaccharides Using 1, 2-O-Ethylidene-α-d-gluco-and-β-d-Mannopyranose as the Acceptors and Acetobromosugars as the Donors via Ortho Ester Intermediates
Qin et al. Chemical synthesis of the Pseudomonas aeruginosa O11 O-antigen trisaccharide based on neighboring electron-donating effect