137410-67-4

Upstream product

• 167466-54-8 methyl 5-O-[(tert-butyl)dimethylsilyl]-β-D-ribofuranoside 
• 1824-96-0 methyl ribofuranoside 
• 137410-53-8 methyl 5-O-(t-butyldimethylsilyl)-3-O-cynnamoyl-2-O-(imidazol-1-yl)thiocarbonyl-β-D-ribofuranoside 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Relevant academic research and scientific papers

Stereoselective Synthesis of Fused Lactones (γ-Butyrolactones) of Sugars and Nucleosides by Free Radical Intramolecular Cyclization

Enantiomerically pure fused lactones of ribofuranosyl sugars and nucleosides at positions 2,3 of the ribofuranose ring have been prepared by intramolecular addition of radicals onto the α-position of α,β-unsaturated esters.

Radical cyclizations on sugar templates: Stereoselective synthesis of fused γ-butyrolactones of carbohydrates

A stereoselective method is described for the synthesis of [3.3.0] fused lactones (γ-butyrolactones) of carbohydrates at the 2 and 3 positions of the furanose ring, by intramolecular addition of radicals onto the α-position of α,β-unsaturared esters. A ne