74211-20-4Relevant academic research and scientific papers
Acid-catalyzed dehydrative cyclization of 4-(D-galacto-pentitol-1-yl)-2-phenyl-2H-1,2,3-triazole. Synthesis and anomeric configuration of D-lyxo-C-nucleoside analogs
Sallam, Mohammed A.E.,Abdel Megid, Somaya M.E.,Townsend, Leroy B.
, p. 53 - 63 (2007/10/03)
Dehydration of 4-(D-galacto-pentitol-1-yl)-2-phenyl-2H-1,2,3-triazole with 20% methanolic sulfuric acid afforded the anomeric pairs of nucleosides, 4-(α-D-lyxopyranosyl)-2-phenyl-2H-1,2,3-triazole (major component) and its β-anomer, as well as 4-(α-D-lyxo
2-phenyl-1,2,3-osotriazole C-nucleoside analogs synthesis and determination of anomeric configuration
Sallam, Mohammed A.E.
, p. 183 - 186 (2007/10/02)
A series of anomeric 2-phenyl-1,2,3-osotriazole C-nucleoside analogs has been prepared. The anomeric configuration was determined by a novel method from the chemical shift of the C-5 proton of the osotriazole base moieties.
STUDIES ON ANHYDRO-OSAZONES. STRUCTURE AND ANOMERIC CONFIGURATION OF THE 3,6-ANHYDRO-OSAZONE DERIVATIVES OBTAINED FROM D-galacto-2-HEPTULOSE PHENYLOSAZONE
Sallam, Mohammed A.E.
, p. 93 - 106 (2007/10/02)
Dehydration of D-galacto-2-heptulose phenylosazone with methanolic sulfuric acid afforded two 3,6-anhydro osazone derivatives (2 and 3).Compound 2 was obtained as the preponderant isomer, without inversion at C-1 (C-3 of the starting osazone), and 3 was o
