679401-23-1

Upstream product

• 679401-21-9 C₁₉H₂₄⁽²⁾H₂O₆ 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 2280-44-6 D-Glucose 
• 679401-20-8 1,2:5,6-di-O-isopropylidene-α-D-allofuranose-3,4-d2 
• 142094-03-9 C₁₂H₁₇⁽²⁾HO₆ 
• 2847-00-9 1,2:5,6-di-O-isopropylidene-α-D-hexofuran-3-ulose 

Downstream Products

• 223470-63-1 3-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranose-3,4,5,5'-2H4 
• 223470-61-9 methyl 3-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranuronate-3,4-d2 
• 223470-59-5 C₁₅H₁₆⁽²⁾H₂O₅ 

Relevant academic research and scientific papers

Studies Towards the Large Scale Chemical Synthesis of the Precursors of Ribonucleosides-3′,4′,5′,5″-2H4 and -2′,3′,4′,5′,5″-2H5

A summary delineating the large scale synthetic studies to prepare labeled precursors of ribonucleosides-3′,4′,5′,5″- 2H4 and -2′,3′,4′,5′,5″ -2H5 from D-glucose is presented. The recycling of deuterium-labeled

Systematic synthesis of specifically 13C/2H-labeled nucleosides from [ul-13C6]-D-glucose

A systematic approach, which combines previously reported reactions with appropriate modifications, was established for preparing a variety of selectively deuterated nucleosides from glucose. We have developed a systematic method of synthesizing specifically deuterated nucleosides from glucose. Selectively 13C/2H-doubly labeled nucleosides, such as [1',2',3',4',5'-13C5;3',5'-2H2]- and [1',2',3',4',5'-13C5;4',5'- H2]-adenosines, have been synthesized starting from [ul-13C6]-D-glucose. These labeled nucleosides are very useful for precise conformational analyses of nucleic acids in solution by heteronuclear multidimensional NMR spectroscopy.