Synthesis of 1-thioaldosides having an amino group at the aglycon terminal
S Chipowsky, CL Yuan
Index: Chipowsky,S.; Lee,Y.C. Carbohydrate Research, 1973 , vol. 31, p. 339 - 346
Full Text: HTML
Citation Number: 85
Abstract
Abstract A number of 1-thio-β-d-aldosides were prepared, directly or indirectly, from acetylated 1-halides of d-galactose, d-glucose, and 2-amino-2-deoxy-d-glucose. These aldosides have an amino group at the terminal position of the aglycon, in the form of 6- aminohexyl, 6-aminohexanoyl, or p-aminophenyl groups.
Related Articles:
Zwitterionic oligonucleotides: a study on binding properties of 2′-O-aminohexyl modifications
[Noe, Christian R.; Winkler, Johannes; Urban, Ernst; Gilbert, Matthias; Haberhauer, Georg; Brunar, Helmut Nucleosides, Nucleotides and Nucleic Acids, 2005 , vol. 24, # 8 p. 1167 - 1185]