92512-29-3

Upstream product

• 6553-96-4 2,4,6-triisopropylphenylsulfonyl chloride 
• 92691-36-6 (2S,4S)-pentane-1,2,3,4-tetraol 
• 457630-79-4 Bis-((R)-2,2-diethyl-[1,3]dioxolan-4-yl)-methanol 
• 684213-72-7 (2S,4S)-di-O-(3,3-pentylidene)-3-deoxyarabitol 
• 684213-89-6 (2R,4R)-di-O-(3,3-pentylidene)-3-O-[(methylthio)thiocarbonyl]arabitol 
• 684213-90-9 (2R,4R)-1,2:4,5-di-O-(3,3-pentylidene)-3-O-[(N-imidazolyl)thiocarbonyl]arabitol 
• 17609-05-1 (2S,4S)-pentane-1,2,4,5-tetraol 
• 79580-65-7 3β-acetoxy-5β-acetoxymethyltetrahydrofuran-2-one 
• 5336-08-3 D-Ribono-1,4-lactone 
• 41162-32-7 2,3,5-tri-O-acetyl-D-ribonic acid γ-lactone 

Downstream Products

• 92512-30-6 (3S,5S)-3,5-bis(benzoyloxy)heptane-1,7-dinitrile 
• 109826-76-8 (+)-<2R(2E,4R),4S,6S,8R,9S>-2-<6-(tert-butyldiphenylsilyloxy)-3,5-dimethyl-2-hexenyl>-8,9-dimethyl-1,7-dioxaspiro<5.5>undecan-4-ol 
• 109826-75-7 (+)-α-<6-(tert-butyldiphenylsilyloxy)-3,5-dimethyl-2-hexenyl>oxiraneethanol 
• 109905-51-3 (2S,4S)-1,2:4,5-dianhydro-3-deoxypentitol 

Relevant academic research and scientific papers

Short synthesis of enantiopure C2-symmetric 1,2:4,5-diepoxypentane and "pseudo"-C2-symmetric 3-azido-1,2:4,5-diepoxypentane from arabitol

On the basis of our previously described selective protection of arabitol as its 1,2:4,5-bis-pentylidene acetal 5, we report a straightforward synthesis of the novel "pseudo"C2-symmetric 3-azido-1,2:4,5-diepoxypentane building block 4 in 6 steps from arab

Enantiospecific total synthesis of L-2',3'-dideoxyisonucleosides via regioselective opening of optically active C2-symmetric 1,4-pentadiene bis- epoxide

A new method for the synthesis of L-2',3'-dideoxyisonucleosides is described. The readily available, optically active C2-symmetric bis-epoxide (2S,4S)-1,2:4,5-diepoxypentane (5) was prepared by a short route from readily available starting mate

A Convenient Procedure for the Deoxygenation and Homologation of D-Ribose Derivatives

5-O-Acetyl- and 5-O-diphenyl-t-butylsilyl-2,3-di-O-acetyl-D-ribonolactones were converted into the corresponding 3-deoxy-2-O-acetyl-D-arabinolactone derivatives (9a) and (9b) by sequential reaction with 1,8-diazabicycloundec-7-ene and hydrogen over