798574-41-1

Upstream product

• 76-83-5 trityl chloride 
• 258336-20-8 2,5-anhydro-3-deoxy-L-talose ethylene acetal 
• 124-63-0 methanesulfonyl chloride 
• 798574-46-6 2,5-anhydro-3-deoxy-6-O-trityl-L-talose ethylene acetal 

Downstream Products

• 798574-42-2 9-((2R,3R,5R)-5-[1,3]Dioxolan-2-yl-2-trityloxymethyl-tetrahydro-furan-3-yl)-9H-purin-6-ylamine 
• 798574-47-7 2-((2R,4R,5R)-4-Azido-5-trityloxymethyl-tetrahydro-furan-2-yl)-[1,3]dioxolane 
• 798574-48-8 1-((2R,3R,5R)-5-[1,3]Dioxolan-2-yl-2-trityloxymethyl-tetrahydro-furan-3-yl)-3-((E)-3-methoxy-acryloyl)-urea 
• 798574-45-5 1-((2R,3R,5R)-5-[1,3]Dioxolan-2-yl-2-trityloxymethyl-tetrahydro-furan-3-yl)-1H-pyrimidine-2,4-dione 
• 798574-44-4 (2R,3R,5R)-5-[1,3]Dioxolan-2-yl-2-trityloxymethyl-tetrahydro-furan-3-ylamine 

Relevant academic research and scientific papers

Ring-expanded analogues of natural oxetanocin: (+) and (-) hydroxymethyl isodideoxyadenosine

New enantiomeric isonucleoside analogues related to natural oxetanocin have been synthesized from D-glucosamine and D-glucose. The structures of the target compounds were confirmed by NMR, HRMS, UV, single crystal X-ray, and optical rotation data. Stabili

Ring-expanded analogues of natural oxetanocin

Synthesis of ring-expanded analogs of the natural compound, oxetanocin is described. The starting material for the synthesis of the series, 4-7, was d-glucosamine and introduction of the base moiety was done through the stereochemically appropriate epoxid