270087-60-0Relevant articles and documents
RETRACTED ARTICLE: Chemical synthesis and antigenic activity of a phosphatidylinositol mannoside epitope from: Mycobacterium tuberculosis
Zhao, Shi-Yuan,Li, Na,Luo, Wan-Yue,Zhang, Nan-Nan,Zhou, Rong-Ye,Li, Chen-Yu,Wang, Jin
, p. 14067 - 14070 (2020/11/21)
Phosphatidylinositol mannosides (PIMs) have been investigated as lipidic antigens for a new subunit tuberculosis vaccine. A non-natural diacylated phosphatidylinositol mannoside (Ac2PIM2) was designed and synthesized by mimicking the natural PIM6 processi
Efficient Synthesis of Unsymmetrical Ureido-Linked Disaccharides
Prosperi, Davide,Ronchi, Silvia,Lay, Luigi,Rencurosi, Anna,Russo, Giovanni
, p. 395 - 405 (2007/10/03)
Five nonsymmetrical urea-linked disaccharides, in which two glycopyranoside units are bound at the 1→2, 1→4, and 1→6 positions, were efficiently synthesized. A mild and safe procedure, in which glycosyl isocyanates were coupled with a glycosylamine, was e
Rapid assembly of oligosaccharides: 1,2-Diacetal-mediated reactivity tuning in the coupling of glycosyl fluorides
Baeschlin, Daniel K.,Green, Luke G.,Hahn, Michael G.,Hinzen, Berthold,Ince, Stuart J.,Ley, Steven V.
, p. 173 - 197 (2007/10/03)
This paper describes the application of 1,2-diacetal protecting groups to control the reactivity tuning of glycosyl fluorides in oligosaccharide coupling reactions. The synthetic potential of this new methodology is demonstrated by the 'one-pot' synthesis