Hendel, 2007 - Google Patents
The synthesis of a Lewis X trisaccharide analogueHendel, 2007
View PDF- Document ID
- 4502450514742499482
- Author
- Hendel J
- Publication year
External Links
Snippet
The synthesis of Lewis X analogue D-Glu-[beta]-1 [right arrow] 4-[L-Fuc-[alpha]-1 [right arrow] 3]-D-GlcNAc-[beta]-(1 [right arrow] O)-Me is described. The synthesis was explored via two routes. Following the first route, fucosylation at O-3 of an'N'-acetylglucosamine …
- 230000015572 biosynthetic process 0 title abstract description 126
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/04—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
- C07H15/10—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical containing unsaturated carbon-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/24—Condensed ring systems having three or more rings
- C07H15/256—Polyterpene radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
- C07H5/04—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium to nitrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/18—Acyclic radicals, substituted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
- C07H5/08—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium to sulfur, selenium or tellurium
- C07H5/10—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium to sulfur, selenium or tellurium to sulfur
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
- C07H13/04—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals attached to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H3/00—Compounds containing only hydrogen atoms and saccharide radicals having only carbon, hydrogen, and oxygen atoms
- C07H3/06—Oligosaccharides, i.e. having three to five saccharide radicals attached to each other by glycosidic linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H3/00—Compounds containing only hydrogen atoms and saccharide radicals having only carbon, hydrogen, and oxygen atoms
- C07H3/04—Disaccharides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/12—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by acids having the group -X-C(=X)-X-, or halides thereof, in which each X means nitrogen, oxygen, sulfur, selenium or tellurium, e.g. carbonic acid, carbamic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H9/00—Compounds containing a hetero ring sharing at least two hetero atoms with a saccharide radical
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Liu et al. | NIS/TMSOTf-promoted glycosidation of glycosyl ortho-hexynylbenzoates for versatile synthesis of O-glycosides and nucleosides | |
Toepfer et al. | An efficient synthesis of the Lewis A (Lea) antigen pentasaccharide moiety | |
Elsaidi et al. | Synthesis of a 1, 3 β-glucan hexasaccharide designed to target vaccines to the dendritic cell receptor, Dectin-1 | |
Lockhoff et al. | Syntheses of glycosylamides as glycolipid analogs | |
Hendel et al. | 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 analogues | |
Crotti et al. | New strategies for the synthesis of bio-medically relevant oligosaccharides: recent updates on 1, 2-cis-O-glycosylation and α-O-sialylation | |
Feng et al. | Synthesis of a Forssman antigen derivative for use in a conjugate vaccine | |
Hsieh et al. | Integrating ReSET with glycosyl iodide glycosylation in step-economy syntheses of tumor-associated carbohydrate antigens and immunogenic glycolipids | |
Hendel | The synthesis of a Lewis X trisaccharide analogue | |
Pickles | The Synthesis of Novel Lewis B and Oncofetal ‘H’Oligosaccharides for Immunological Studies | |
Mutoni | Synthesis of the Tetrasaccharide GlcNAcLex Fragment of Tumor Associated Carbohydrate Antigen Dimeric Lewis X | |
Asnani et al. | Synthesis of Lewis X trisaccharide analogues in which glucose and rhamnose replace N-acetylglucosamine and fucose, respectively | |
Liao | Synthesis and conformational analysis of Lewis A analogues en route to the synthesis of Lewis A-Lewis X neoglycoprotein | |
Kuir | Synthesis of Tetrasaccharide and Pentasaccharide Fragments of the Tumor-Associated Carbohydrate Antigen Lewis A Lewis X | |
Davidson | Synthesis of selected fragments of the Lewis B Lewis A Tumor-Associated Carbohydrate Antigen | |
Homayonia et al. | Epoxide‐Mediated Trans‐Thioglycosylation and Application to the Synthesis of Oligosaccharides Related to the Capsular Polysaccharides of C. jejuni HS: 4 | |
Bhetuwal | Stereoselective Synthesis of β-Mannosides and β-Mannosamines Via Cs2Co3-Mediated Anomeric O-Alkylation | |
Gattoji | Total Synthesis of Tumor Associated Carbohydrate Antigen β-Aminooxy GM2 | |
Moore | Synthesis of Lewis X Analogues and Their Use as Inhibitors in Competitive Binding Studies | |
Keith | Total Synthesis of the Morganella Morganii Zwitterionic Polysaccharide Repeating Unit | |
Boltje et al. | Controlling anomeric selectivity, reactivity, and regioselectivity in glycosylations using protecting groups | |
Wang | Synthesis of a Lewis X trisaccharide glycoconjugate and competitive binding studies with Lewis X analogues | |
Mickael | Total Synthesis of the Tumor-Associated Carbohydrate Antigen Lewis A Lewis X Hexasaccharide and Selected Fragments | |
Nejatie | Iterative Synthesis of Tetra-and Pentasaccharide Fragments of the Dimeric Lewis X Tumor-Associated Carbohydrate Antigen | |
Gast | Synthesis of fluorinated S. pneumoniae serotype 8 glycotope mimetics for the assembly of synthetic vaccine candidates and a set of rhamnosylation-specific antibodies enables the detection of novel protein glycosylation in bacteria |