259746-24-2

Upstream product

• 4005-49-6 N-benzoyladenine 
• 94933-92-3 3-O-Acetyl-1,2-O-isopropyliden-D-glucofuranose-5,6-sulfit 
• 259746-20-8 3,6-anhydro-1,2-O-isopropylidene-5-O-pivaloyl-α-D-glucofuranose 
• 27821-03-0 3,6-Anhydro-1,2-O-isopropyliden-α-D-glucofuranose 

Downstream Products

• 259746-28-6 N⁶-benzoyl-9-(3',6'-anhydro-2'-deoxy-5'-O-pivaloyl-β-D-glucofuranosyl)-adenine 
• 259746-26-4 N⁶-benzoyl-9-(3',6'-anhydro-5'-O-pivaloyl-β-D-glucofuranosyl)-adenine 

Relevant academic research and scientific papers

Synthesis of 3,6-anhydro sugars from cyclic sulfites and sulfates and their applications in the preparation of bicyclonucleoside analogues of ddC and ddA

Cyclic sulfates 21-23 and sulfite 27 derived from glucofuranose lead to the 3,6-anhydrosugar 28 in excellent yields when treated with sodium sulfite or in basic media. When treated with sodium sulfite, the 3-deoxy derivative 24 fails to give the intramolecular cyclization which leads to the anhydrosugars. Instead it gives the disulfonate derivative 26. 28 was used as starting material to prepare bicyclonucleosides 43 and 46, which are analogues of the anti-HIV agents ddC and ddA.