6160-54-9

Upstream product

• 100-39-0 benzyl bromide 
• 51255-17-5 1-O-methyl-2-deoxy-D-ribofuranoside 
• 922-65-6 divinylcarbinol 
• 100-44-7 benzyl chloride 
• 120132-09-4 Benzoic acid (2R,3S)-3-benzyloxy-2-hydroxy-pent-4-enyl ester 
• 120132-10-7 (2R,3S)-1,3-di-O-benzyl-4-pentene-1,2,3-triol 
• 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 
• 221216-38-2 (2R,3R)-2-((benzyloxy)methyl)-3-vinyloxirane 
• 212579-64-1 (4R)-1-(2,2-dimethyl-[1,3]dioxolan-4-yl)allyl alcohol 
• 34212-65-2 Methyl 2-Deoxy-3-benzyl-D-ribofuranoside 
• 452-51-7 D-2-deoxyribose 

Downstream Products

• 133658-23-8 (2R,3S)-3-(benzyloxy)-2-(benzyloxymethyl)-5-(phenylthio)tetrahydrofuran 
• 861100-51-8 3,5-di-O-benzyl-2-deoxy-β-D-erythropentofuranosyl hydroperoxide 
• 861100-48-3 3,5-di-O-benzyl-2-deoxy-α-D-erythropentofuranosyl hydroperoxide 

Relevant academic research and scientific papers

Synthesis and Antiviral Activity of Acyclic Nucleosides with a 3(S),5-Dihydroxypentyl of 4(R)-Methoxy-3(S),5-dihydroxypentyl Side Chain

Optically pure acyclic nucleoside analogues with a 3(S),5-dihydroxypentyl or 4(R)-methoxy-3(S),5-dihydroxypentyl side chain were synthesized starting from 2-deoxy-D-ribose.The acyclic nucleosides were obtained by alkylation of the bases with the mesylates

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.