51842-38-7Relevant articles and documents
3-Butenyloxycarbonyl as a new hydroxyl protecting group in carbohydrate synthesis
Zeng, Nana,Niu, Youhong,Ye, Xin-Shan
supporting information, p. 2935 - 2938 (2016/06/14)
3-Butenyloxycarbonyl (Bloc) has been identified as a new hydroxyl protecting group, which can be introduced under mild conditions in high yields and selectively removed by OsO4/NaIO4/2,6-lutidine in CH3CN-H2O wi
Disaccharide-containing macrocycles by click chemistry and intramolecular glycosylation
Tiwari, Vinod K.,Kumar, Amit,Schmidt, Richard R.
, p. 2945 - 2956 (2012/07/27)
In this study o- and m-xylylene moieties in combination with a triazolylmethyl moiety have been successfully employed as a relatively rigid spacer system in intramolecular glycosylation reactions. Phenyl 3,4,6-tri-O-benzyl-2-O-propargyl-1-thio-D-glucopyra
A reversal in the order of H-6R and H-6S chemical shifts of some aldohexopyranose derivatives, associated with the acetylation of OH-4 and OH-6 groups. A distinction between 3- and 4-linked D-glucose residues in disaccharides
Rao, Vanga S.,Perlin, Arthur S.
, p. 2688 - 2694 (2007/10/02)
On peracetylation of methyl α- or β-D-glucopyranose, there is a reversal in the order of the chemical shifts of the 6,6'-methylene protons, i.e., whereas the H-6S signal appears downfield of H-6R in the spectra of the glucosides, the