Solid-Phase Synthesis of α-(2-(Benzylthio)- 1,4-dihydro-6-methyl-4-p-tolylpyrimidine-5- carboxamido) Acids:  a New Strategy To Create Diversity in Heterocyclic Scaffolds

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Tariq M. Rana
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Biopolymers ◽  
1981 ◽  
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Shi-Zhen Yang ◽  
An-Qing Ma ◽  
Yun-Neng Chen ◽  
Yong-Qing Jiang ◽  
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ChemInform ◽  
2010 ◽  
Vol 23 (42) ◽  
pp. no-no
Author(s):  
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S. PETERS ◽  
M. MELDAL ◽  
K. BOCK ◽  
H. PAULSEN

Tetrahedron ◽  
2006 ◽  
Vol 62 (6) ◽  
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Thomas Berthelot ◽  
Mario Gonçalves ◽  
Georges Laïn ◽  
Karine Estieu-Gionnet ◽  
Gérard Déléris

Catalysts ◽  
2020 ◽  
Vol 10 (11) ◽  
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Lishi Ren ◽  
...  

6′/3′-Sialylated N-acetyllactosamine (6′/3′-SLN) is important for discrimination of the source (human or avian) of influenza virus strains. Biotinylated oligosaccharides have been widely used for analysis and quick detection. The development of efficient strategies to synthesize biotin-tagged 6′/3′-SLN have become necessary. Effective mixing is essential for enzymatic solid-phase oligosaccharide synthesis (SPOS). In the current study, newly developed technology ultrahigh-frequency-acoustofluidics (UHFA), which can provide a powerful source for efficient microfluidic mixing, solid-phase oligosaccharide synthesis and one-pot multienzyme (OPME) system, were used to develop a new strategy for oligosaccharide synthesis. Firstly, biotinylated N-acetylglucosamine was designed and chemically synthesized through traditional approaches. Secondly, biotinylated 6′- and 3′-sialyl-N-acetylglucosamines were prepared in solution through two sequential OPME modules in with a yield of ~95%. Thirdly, 6′-SLN was also prepared through UHFA-based enzymatic solid-phase synthesis on magnetic beads with a yield of 64.4%. The current strategy would be potentially used for synthesis of functional oligosaccharides.


Synfacts ◽  
2006 ◽  
Vol 2006 (6) ◽  
pp. 0621-0621
Author(s):  
G. Déléris ◽  
T. Berthelot ◽  
M. Gonçalves ◽  
G. Laïn ◽  
K. Estieu-Gionnet

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