111138-00-2

Upstream product

• 35784-67-9 1,2:5,6-di-O-isopropylidene-3-C-methyl-α-D-glucofuranose 
• 100-39-0 benzyl bromide 
• 53270-26-1 (3aR,5R,6S,6aR)-5-[(4R)-2,2-dimethyl[1,3]dioxolan-4-yl]-2,2,6-trimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol 
• 53270-27-2 C₁₃H₂₀O₆ 

Downstream Products

• 55533-86-3 3-O-benzyl-1,2-O-isopropylidene-3-C-methyl-α-D-glucofuranose 
• 1330658-72-4 C₂₀H₂₆N₂O₁₁S₂ 
• 1217483-40-3 C₂₀H₂₄N₂O₁₁S₂ 
• 1217483-13-0 C₁₉H₂₂N₂O₈S 
• 1217483-14-1 C₂₀H₂₂N₂O₇ 
• 1217483-16-3 C₃₂H₃₂N₂O₈ 
• 1217483-17-4 C₄₁H₄₉N₄O₉P 
• 120615-67-0 3-O-benzyl-3-C-methyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 1217483-12-9 C₂₂H₂₈N₂O₁₂S₂ 
• 1330658-69-9 C₉H₁₂O₄ 
• 1217483-10-7 C₁₇H₂₄O₆ 
• 1217483-11-8 C₁₉H₂₈O₁₀S₂ 
• 120594-95-8 3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-3-C-methyl-α-D-xylohexo-5-eno-furanose 
• 120595-02-0 (2S,3R,4R,5R)-4-Benzyloxy-5-ethyl-4-methyl-tetrahydro-furan-2,3-diol 

Relevant academic research and scientific papers

Synthesis and biophysical evaluation of 3′-Me-α-l-LNA - Substitution in the minor groove of α-l-LNA duplexes

The synthesis and biophysical evaluation of 3′-Me-α-l-LNA is reported. The synthesis of the nucleoside building block phosphoramidite was accomplished starting from diacetone glucose. The 3′-Me group was introduced in the desired configuration by hydride