70448-45-2Relevant academic research and scientific papers
Facile synthesis of oxo-/thioxopyrimidines and tetrazoles C-C linked to sugars as novel non-toxic antioxidant acetylcholinesterase inhibitors
Figueiredo,Ismael,Pinheiro,Silva,Justino,Silva,Goulart,Mira,Araújo,Campoy,Rauter
, p. 47 - 54 (2012/02/05)
Microwave-assisted synthesis of oxo-/thioxopyrimidines and tetrazoles linked to furanoses with d-xylo and d-ribo configuration, and to a d-galacto pyranose is reported and compared to conventional methods. Reaction of dialdofuranoses and dialdopyranoses w
New one-carbon degradative transformation of β-alkyl-β-azido alcohols
Fan, Qiu-Hua,Ni, Nan-Ting,Li, Qin,Zhang, Li-He,Ye, Xin-Shan
, p. 1007 - 1009 (2007/10/03)
A new transformation of 2-azido-1-hydroxy-containing compounds to nitriles with one carbon less than the starting materials by oxidation was reported. The reaction can be performed under mild conditions.
Bioactive pseudo-C-nucleosides containing thiazole, thiazolidinone, and tetrazole rings
Rauter, Amelia P.,Padilha, Maria,Figueiredo, Jose A.,Ismael, Maria I.,Justino, Jorge,Ferreira, Humberto,Ferreira, Maria J.,Rajendran, Candasamy,Wilkins, Richard,Vaz, Pedro D.,Calhorda
, p. 275 - 296 (2007/10/03)
The synthesis of new pseudo-C-nucleosides was accomplished starting from 3-O-benzyl-1,2-O-isopropylidene-α-D-ribo-pentodialdo-1,4-furanose, aiming to build thiazole, triazole, tetrazole, and thiazolidinone derivatives. The stereochemistry of the thiazolid
