430436-33-2Relevant academic research and scientific papers
Configuration and conformation of a novel uridine analogue: 1H and 13C NMR spectra of (5′S)-1-[2′ -(2-hydroxyethyl)tetrahydropyran-5′-yl]-1H-pyrimidine-2,4-dione
Balayiannis, George,Papaioannou, Dionissios,Troganis, Anastassios
, p. 244 - 246 (2002)
A combination of homo- and heteronuclear 1D and 2D NMR techniques provided the assignment of the 1H and 13C resonances of the major component of a reaction product consisting of the two possible diastereomers of (5′S)-1-[2′-(2-hydroxyethyl)tetrahydropyran-5′-yl] -1H-pyrimidine-2,4-dione and showed that the tetrahydropyranyl ring in the major 5′S,2′S-isomer adopts the twist conformation. Copyright
