358738-50-8Relevant articles and documents
Synthesis of substituted 2-(β-d-glucopyranosyl)-benzimidazoles and their evaluation as inhibitors of glycogen phosphorylase
Bokor, éva,Szilágyi, Eniko,Docsa, Tibor,Gergely, Pál,Somsák, László
, p. 179 - 186 (2013/11/19)
Microwave assisted condensation of O-perbenzoylated C-(β-d- glucopyranosyl)formic acid with 1,2-diaminobenzenes in the presence of triphenylphosphite gave the corresponding O-protected 2-(β-d- glucopyranosyl)-benzimidazoles in moderate yields. O-Perbenzoy
Preparation of 3,5-bis-(β-D-glycopyranosyl)-1,2,4-thiadiazoles from C-(β-D-glycopyranosyl)thioformamides
Osz,Czifrák,Deim,Szilágyi,Bényei,Somsák
, p. 5429 - 5434 (2007/10/03)
Acylated C-glycopyranosyl thioformamides of D-gluco, D-galacto, and D-xylo configuration were obtained by treating the corresponding glycosyl cyanides with hydrogen sulfide in the presence of triethylamine. The thioformamides gave 3,5-bis-(β-D-glycopyranosyl)-1,2,4-thiadiazoles in reactions with potassium bromate and sodium dithionite in dichloromethane-water biphasic solvent mixture. Deprotected derivatives were prepared by Zemple?n deacylation.