7473-44-1Relevant academic research and scientific papers
Synthesis of a Tridecasaccharide Lipooligosaccharide Antigen from the Opportunistic Pathogen Mycobacterium kansasii
Bai, Bing,Liu, Yu-Hsuan,Lowary, Todd L.,Shen, Ke
supporting information, p. 24859 - 24863 (2021/10/25)
The outer surfaces of mycobacteria, including the organism that causes tuberculosis, are decorated with an array of immunomodulatory glycans. Among these are lipooligosaccharides (LOSs), a class of molecules for which the function remains poorly understoo
Synthesis of glyceryl glycosides related to A-type prymnesin toxins
Hems, Edward S.,Nepogodiev, Sergey A.,Rejzek, Martin,Field, Robert A.
supporting information, p. 14 - 23 (2018/05/03)
A suite of glycosylated glycerol derivatives representing various fragments of the glycosylated ichthyotoxins called prymnesins were chemically synthesised. Glycerol was used to represent a small fragment of the prymnesin backbone, and was glycosylated at
Synthesis of two natural betulinic acid saponins containing α-l-rhamnopyranosyl-(1→2)-α-l-arabinopyranose and their analogues
Gauthier, Charles,Legault, Jean,Lavoie, Serge,Rondeau, Simon,Tremblay, Samuel,Pichette, André
, p. 7386 - 7399 (2008/12/20)
A concise synthesis of naturally occurring betulinic acid saponins bearing an α-l-rhamnopyranosyl-(1→2)-α-l-arabinopyranoside moiety at the C-3 position is described. Betulinic acid 3β-O-α-l-rhamnopyranosyl-(1→2)-[β-d-glucopyranosyl- (1→4)]-α-l-arabinopyr
