34212-65-2

Upstream product

• 67-56-1 methanol 
• 128057-04-5 (3R,4S)-3-O-benzyl-4,5-O-isopropylidene-3,4,5-trihydroxypentanal 
• 128057-00-1 (3R,4R)-3-O-benzyl-4,5-O-isopropylidene-3,4,5-trihydroxypentanal 
• 51255-17-5 1-O-methyl-2-deoxy-D-ribofuranoside 
• 100-44-7 benzyl chloride 
• 212579-64-1 (4R)-1-(2,2-dimethyl-[1,3]dioxolan-4-yl)allyl alcohol 
• 105386-65-0 methyl 5-O-(tert-butyldimethylsilyl)-2-deoxy-α,β-D-erythropentofuranoside 
• 105386-66-1 methyl 3-O-benzyl-5-O-(t-butyldimethylsilyl)-2-deoxyribofuranoside 
• 128111-95-5 (2R,3R)-2-<2-O-benzyl-3,4-O-isopropylidene-2,3,4-trihydroxybut-1-yl>-1,3-dithiane 
• 128112-01-6 (2R,3S)-2-<2-O-benzyl-3,4-O-isopropylidene-2,3,4-trihydroxybut-1-yl>-1,3-dithiane 
• 128112-00-5 (2R,3S)-2-<3,4-O-isopropylidene-2,3,4-trihydroxybut-1-yl>-1,3-dithiane 
• 120132-09-4 Benzoic acid (2R,3S)-3-benzyloxy-2-hydroxy-pent-4-enyl ester 
• 115586-67-9 (2R,3S)-3-O-benzyl-4-pentene-1,2,3-triol 
• 108275-52-1 (+)-(3S,4R)-3-benzyloxy-4,5-O-isopropylidene-4,5-dihydroxy-1-pentene 

Downstream Products

• 6160-55-0 methyl 3,5-di-O-benzyl-2-deoxy-β-D-erythro-pentofuranoside 
• 6160-54-9 methyl 3,5-di-O-benzyl-2-deoxy-α-D-erythro-pentofuranoside 
• 189291-00-7 Diethyl-thiocarbamic acid O-((2R,3S)-3-benzyloxy-5-methoxy-tetrahydro-furan-2-ylmethyl) ester 
• 149284-21-9 C₁₃H₁₇N₃O₃ 
• 149284-22-0 C₁₃H₁₇N₃O₃ 
• 189290-91-3 α-2'-deoxy-3'-O-benzyl-5'-O-diethylthiocarbamoyluridine 
• 189290-89-9 2-deoxy-1-O-acetyl-3-O-benzyl-5-O-diethylthiocarbamoyl-D-ribofuranoside 

Relevant academic research and scientific papers

Highly stereoselective synthesis of 2'-deoxy-α-ribonucleosides and 2-deoxy-α-C-ribofuranosides by remote stereocontrolled glycosylation

A new and efficient method for catalytic highly α-selective N-and C-glycosylations of 2-deoxyribose derivative with various trimethylsilylated nucleophiles was successfully developed by utilizing effective remote stereocontrol with 5-O-diethylthio carbamo

Chemistry of L-Ascorbic and D-Isoascorbic Acids. An Efficient Synthesis of 2-Deoxypentofuranoses

L-Ascorbic and D-isoascorbic acids have been converted to methyl 3-O-benzyl-2-deoxypentofuranosides.The synthetic routes are enantiospecific, efficient, and economic and proceed in high yields.

A NEW SYNTHETIC METHOD FOR γ-BUTYROLACTOLS BY THE PALLADIUM-CATALYZED REGIOSELECTIVE OXIDATION OF 1-ALKEN-4-OLS

3-substituted 1-alken-4-ols were oxidized with PdCl2-benzoquinone regioselectively at the terminal carbon to afford cyclic hemiacetals (γ-butyroacetols), which were converted to γ-butiroacetones by the Jones oxidation.This reactions was applied to the synthesis of optically active deoxyribose and γ-butenolides.

2-deoxypentose derivatives

PAF analogues derived from 2-deoxyribose or 2-deoxyxylose, having cytotoxic, hypotensive and PAF agonist/antogonist properties.