380883-52-3

Upstream product

• 874-60-2 4-methyl-benzoyl chloride 
• 55775-39-8 1-O-methyl-3,5-di-O-benzyl-D-ribofuranoside 

Downstream Products

• 380883-58-9 1-O-acetyl-2,3,5-tri-O-(4-toluoyl)-α/β-D-ribofuranose-2-2H1 
• 380883-57-8 1-O-methyl-2,3,5-tris-O-(4-methylbenzoyl)-β-D-[2-2H1]ribofuranose 
• 380883-54-5 methyl 3,5-di-O-benzyl-2-O-(trifluoromethyl)sulfonyl-β-D-[2-2H1]arabinofuranoside 
• 380883-55-6 3,5-di-O-benzyl-1-O-methyl-2-O-propanoyl-β-D-[2-2H1]ribofuranose 
• 380883-56-7 3,5-di-O-benzyl-1-O-methyl-β-D-[2-2H]ribofuranose 
• 380883-53-4 3,5-di-O-benzyl-1-O-methyl-β-D-[2-2H1]arabinofuranose 

Relevant academic research and scientific papers

Synthesis of [2′-2H1]-Ribonucleosides

New syntheses of C(2′)-deuterated ribonucleosides have been accomplished starting either from 3,5-di-O-benzyl-1-O-methyl-α,β -D-ribofuranose (1b) or 2,3-O-isopropylidene-D-ribose (14), with >97 atom-% D incorporation in both cases. The former is suited to

Studies on the stereoselective synthesis of deuterated D-ribose derivatives

In view of the importance of the site-specific substitution of the H-atom by its stable isotope 2H in a stereoselective/stereospecific manner at the pentose sugar residue, decreasing the spectral overcrowding in various regions of 1D and 2D hom

Synthetic studies to improve the deuterium labelling in nucleosides for facilitating structural studies of large RNAs by high-field NMR spectroscopy

Synthetic studies to prepare ribonucleosides deuterated at C2′ and the application of the developed procedures for the synthesis of 2H5-ribonucleosides from 1,2-O-isopropylidene-3-O-benzyl-ribofuranose-3,4,5,5′ -2H4/