70363-52-9Relevant articles and documents
Synthesis and structure of the hypermodified nucleoside of rat liver phenylalanine transfer ribonucleic Acid.
Itaya, Taisuke,Kanai, Tae
, p. 1318 - 1326 (2007/10/03)
The first synthesis of (alphaS,betaS)-beta-hydroxy-alpha-[(methoxycarbonyl)amino]-4,6-dimethyl-9-oxo-3-beta-D-ribofuranosyl-4,9-dihydro-3H-imidazo[1,2-a]purine-7-butanoic acid methyl ester [(alphaS,betaS)-11] has been achieved by OsO(4) oxidation of [S-(E
Synthesis of [R-(R*,S*)]- and [S-(R*,R*)]-β-Hydroxy-3-(β-D-ribofuranosyl)- wybutines, the most probable alternatives for the hypermodified nucleoside of rat liver phenylalanine transfer ribonucleic acid
Itaya, Taisuke,Kanai, Tae,Iida, Takehiko
, p. 1979 - 1982 (2007/10/03)
The synthesis of the title compounds started with the Vilsmeier reaction of 3-[2,3,5-tris-O-(tert-butyldimethylsilyl)-β-D- ribofuranosyl]wye (5b) and proceeded through the Wittig reaction with (R)-N-(methoxycarbonyl)-3-(triphenylphosphonio)alaninate (4), methylation with trimethylsilyldiazomethane, OsO4 oxidation, cyclocondensation with triphosgene, and catalytic hydrogenolysis. Chromatographic separation of the resulting diastereomeric mixture and subsequent deprotection afforded the two desired nucleosides [[R-(R*,S*)]- and [S-(R*,R*)]-2b] for the first time.
SYNTHESIS OF OPTICALLY ACTIVE FORMS OF HYDROXY-Y BASE, THE MINOR COMPONENT OF RAT LIVER PHENYLALANINE TRANSFER RIBONUCLEIC ACID
Itaya, Taisuke,Watanabe, Nobuhide,Mizutani, Akemi
, p. 4043 - 4046 (2007/10/02)
-β-Hydroxywybutine (6) and its -isomer (9) have been synthesized as the most probable alternatives for hydroxy-Y base isolated from rat liver phenylalanine tRNA.