Chittaboina et al., 2005 - Google Patents
One-pot synthesis of triazole-linked glycoconjugatesChittaboina et al., 2005
- Document ID
- 5937596873921813299
- Author
- Chittaboina S
- Xie F
- Wang Q
- Publication year
- Publication venue
- Tetrahedron letters
External Links
Snippet
Highly efficient one-pot synthesis of 1, 2, 3-triazole-linked glycoconjugates was presented involving a Cu (I) catalyzed 1, 3-dipolar cycloaddition as the key step. It offers a convenient route to prepare neoglycoconjugates derived from unprotected saccharides or peracetylated …
- 238000005580 one pot reaction 0 title abstract description 13
Classifications
-
- 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
- C07H19/06—Pyrimidine radicals
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
- C07H21/02—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with ribosyl as saccharide radical
-
- 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- C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
-
- 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
-
- 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
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Chittaboina et al. | One-pot synthesis of triazole-linked glycoconjugates | |
| Wilkinson et al. | Synthetic utility of glycosyl triazoles in carbohydrate chemistry | |
| Sakagami et al. | A selective ring opening reaction of 4, 6-O-benzylidene acetals in carbohydrates using trialkylsilane derivatives | |
| Kushwaha et al. | Click reaction in carbohydrate chemistry: recent developments and future perspective | |
| Lee et al. | Synthesis of multivalent neoglyconjugates of MUC1 by the conjugation of carbohydrate-centered, triazole-linked glycoclusters to MUC1 peptides using click chemistry | |
| Li et al. | Gold (I)-catalyzed glycosylation with glycosyl ynenoates as donors | |
| Esposito et al. | Automated synthesis of sialylated oligosaccharides | |
| Bhunia et al. | Design, Synthesis, and Evaluation of Novel 1, 2, 3‐Triazole‐Tethered Glycolipids as Vaccine Adjuvants | |
| de Paz et al. | Synthesis of a Ley neoglycoconjugate and Ley-functionalized gold glyconanoparticles | |
| Salamone et al. | Programmed chemo-enzymatic synthesis of the oligosaccharide component of a carbohydrate-based antibacterial vaccine candidate | |
| WO2012069188A1 (en) | Continuous flow processes for photoconjugation of high-molecular chemical entities | |
| Pozsgay | A new strategy in oligosaccharide synthesis using lipophilic protecting groups: synthesis of a tetracosasaccharide | |
| Chen et al. | Synthesis of a C3-symmetric (1→ 6)-N-acetyl-β-D-glucosamine octadecasaccharide using click chemistry | |
| Gadikota et al. | Synthesis of oligosaccharide fragments of mannosylated lipoarabinomannan appropriately functionalized for neoglycoconjugate preparation | |
| JPH11508564A (en) | Methods for producing synthetic N-linked glycoconjugates | |
| Loskot et al. | Nucleophilic catalysis of meon-neoglycoside formation by aniline derivatives | |
| Wang et al. | Palladium-Catalyzed Stereospecific Glycosylation Enables Divergent Synthesis of N–O-Linked Glycosides | |
| Qin et al. | Chemical synthesis of the Pseudomonas aeruginosa O11 O-antigen trisaccharide based on neighboring electron-donating effect | |
| US20080194801A1 (en) | Robust multidentate ligands for diagnosis and anti-viral drugs for influenza and related viruses | |
| Pergolizzi et al. | Contemporary glycoconjugation chemistry | |
| Sarkar et al. | Synthesis of the trisaccharide repeating unit of the O‐antigen related to the enterohemorrhagic Escherichia coli Type O26: H | |
| Oikawa et al. | Simple formylacetal (CH2) as a novel linker for saccharide synthesis on soluble-polymer support | |
| Paul et al. | Synthesis of novel glycolipids derived from glycopyranosyl azides and N-(β-glycopyranosyl) azidoacetamides | |
| Saksena et al. | Conjugating low molecular mass carbohydrates to proteins 1. Monitoring the progress of conjugation | |
| JP4942014B2 (en) | O-linked sugar amino acids |