94426-71-8

Upstream product

• 5754-34-7 4-(2-hydroxyethyl)-2,2-dimethyl-1,3-dioxolane 
• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 3068-00-6 D,L-1,2,4-butanetriol 

Downstream Products

• 71998-69-1 (+/-)-4-benzyloxy-butane-1,2-diol 
• 171110-94-4 4-<(2-benzyloxy)ethyl>-1,3-dioxolan-2-one 
• 185155-48-0 4-benzyloxy-1-hydroxybutan-2-one 
• 186090-92-6 [3-(2-Benzyloxy-ethyl)-3H-diazirin-3-yl]-methanol 
• 186090-91-5 4-benzyloxy-1-triphenylmethyloxy-2-butanone 
• 186090-90-4 (+/-)-4-benzyloxy-1-triphenylmethyloxy-2-butanol 
• 186090-93-7 2-azi-4-benzyloxy-1-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyloxy)butane 
• 19790-60-4 3-Benzyloxypropanal 
• 94426-72-9 2-(2-(benzyloxy)ethyl)oxirane 
• 94426-80-9 1-<4-(benzyloxy)-2-oxobutyl>thymine 
• 94426-79-6 1-<4-benzyloxy)-2-oxobutyl>uracil 
• 94426-76-3 1-<4-(benzyloxy)-2-hydroxybutyl>thymine 
• 94426-75-2 1-<4-(benzyloxy)-2-hydroxybutyl>uracil 
• 94426-74-1 9-<4-(benzyloxy)-2-hydroxybutyl>adenine 

Relevant academic research and scientific papers

Condensation of 1,2,4-Butanetriol with Carbonyl Compounds and Reactions of Hydroxyalkyl-1,3-dioxacyclanes

A mixture of isomers of 2-(1,3-dioxolan-4-yl)ethanol and 1,3-dioxan-4-ylmethanol was prepared by reaction of 1,2,4-butanetriol with paraformaldehyde. This mixture was subjected to O-alkylation, O-acylation, condensation with phenyl isocyanate, and substitution of OH groups for Cl. The relative activity of acetone derivatives of glycerol and 1,2,4-butanetriol in reactions with allyl chloride and benzyl chloride was estimated.

Role of hydroxymethyl group as a new hydrophilic 4'-pocket in 5'-norcarbocyclic nucleoside analogues

Steric and electronic parameters of 4'-substituents play significant roles in steering the conformation of nucleoside analogues. In order to investigate the relationship of 4'-group with antiviral enhancement, novel 4'-hydroxymethyl- 5'-norcarbocyclic ade

Synthesis of diether-linked cationic lipids for gene delivery

Quaternary ammonium lipids 1b-d, with diether linkages between hydrocarbon chains and butane or hexane backbone, were synthesized for cationic liposome-mediated gene delivery. The synthetic strategy of using C- 4 or C-6 synthon permits the achievement of the variation of the hydrophobic domain as well as changes of space between the quaternary ammonium head and the hydrophobic domain in the diether-linked cationic lipids.

Synthesis and application of α-D-mannosyl clusters as photoaffinity ligands for mannose-binding proteins: Concanavalin A as a model receptor

Mono-, di-, and tri-antennary α-D-mannopyranosyl derivatives were synthesized as oligosaccharide mimics. The compounds vary in the length of the acyclic aglyconic spacers linking, in the case of the di- and tri-antennary derivatives, the glycosyl endgroup