79781-69-4Relevant articles and documents
A novel and convenient method for the removal of a nitrate group at the anomeric position
Gauffeny, Francoise,Marra, Alberto,Shun, Lian Kiow Shi,Sinay, Pierre,Tabeur, Christine
, p. 237 - 240 (1991)
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Reagent controlled glycosylations for the assembly of well-defined pel oligosaccharides
Codeé, Jeroen D.C.,Wang, Liming,Zhang, Yongzhen,Overkleeft, Herman S.,van der Marel, Gijsbert A.
, p. 15872 - 15884 (2021/01/19)
A new additive, methyl(phenyl)formamide (MPF), is introduced for the glycosylation of 2-azido-2-deoxyglucose building blocks. A linear α-(1,4)-glucosamine tetrasaccharide was assembled to prove the utility of MPF. Next, a hexasaccharide fragment of the Pseudomonas aeruginosa exopolysaccharide Pel was assembled using a [2 + 2 + 2] strategy modulated by MPF. The used [galactosazide-α-(1,4)-glucosazide] disaccharide building blocks were synthesized using a 4,6-O-DTBS protected galactosyl azide donor.
Conversion of glycals into vicinal-1,2-diazides and 1,2-(or 2,1)-azidoacetates using hypervalent iodine reagents and Me3SiN3. Application in the synthesis of: N -glycopeptides, pseudo-trisaccharides and an iminosugar
Chennaiah, Ande,Bhowmick, Srijita,Vankar, Yashwant D.
, p. 41755 - 41762 (2017/09/08)
Glycals were found to react with a reagent system comprising of phenyliodine bis(trifluoroacetate) (PIFA) and Me3SiN3 in the presence of TMSOTf as a catalyst to form the corresponding vicinal 1,2-diazides. On the other hand, they rea