862201-11-4Relevant academic research and scientific papers
Halogen-substituted (C-β-d-glucopyranosyl)-hydroquinone regioisomers: Synthesis, enzymatic evaluation and their binding to glycogen phosphorylase
Alexacou, Kyra-Melinda,Zhang, Yun Zhi,Praly, Jean-Pierre,Zographos, Spyros E.,Chrysina, Evangelia D.,Oikonomakos, Nikos G.,Leonidas, Demetres D.
scheme or table, p. 5125 - 5136 (2011/10/09)
Electrophilic halogenation of C-(2,3,4,6-tetra-O-acetyl-β-d- glucopyranosyl) 1,4-dimethoxybenzene (1) afforded regioselectively products halogenated at the para position to the d-glucosyl moiety (8, 9) that were deacetylated to 3 (chloride) and 16 (bromid
In the search of glycogen phosphorylase inhibitors: Synthesis of C-D-glycopyranosylbenzo(hydro)quinones - Inhibition of and binding to glycogen phosphorylase in the crystal
He, Li,Yun, Zhi Zhang,Tanoh, Marcelle,Chen, Guo-Rong,Praly, Jean-Pierre,Chrysina, Evangelia D.,Tiraidis, Costas,Kosmopoulou, Magda,Leonidas, Demetres D.,Oikonomakos, Nikos G.
, p. 596 - 606 (2007/10/03)
Penta-O-acetyl-β-D-glycopyranoses and 1,4-dimethoxybenzene led selectively by electrophilic substitution to C-β-D-glycopyranosyl-1,4- dimethoxybenzenes which were converted by simple and efficient reactions (oxidation, reduction and deacetylation) to the
C-Glycopyranosyl-1,4-benzoquinones and -hydroquinones opening access to C-glycosylated analogs of vitamin E
Praly, Jean-Pierre,He, Li,Bing, Bing Qin,Tanoh, Marcelle,Chen, Guo-Rong
, p. 7081 - 7085 (2007/10/03)
2-(Per-O-acetyl-β-D-glycopyranosyl)-1,4-dimethoxybenzenes led to C-glycosyl-hydroquinones suitable for preparing C-glycosylated analogs of vitamin E, having the sugar moiety free or acetylated.
