94426-71-8

Upstream product

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

Downstream Products

• 1312706-50-5 (+/-)-[3-(t-butyldimethylsilanyloxy)-3-(t-butyldimethylsilanyloxymethyl)pent-4-enyloxymethyl]benzene 
• 1312706-49-2 (+/-)-5-benzyloxy-3-(t-butyldimethylsilanyloxymethyl)pent-1-en-3-ol 
• 1312706-48-1 4-benzyloxy-1-(t-butyldimethylsilanyloxy)-butan-2-one 
• 171110-94-4 4-<(2-benzyloxy)ethyl>-1,3-dioxolan-2-one 
• 71998-69-1 (+/-)-4-benzyloxy-butane-1,2-diol 
• 94426-77-4 9-<4-(benzyloxy)-2-oxobutyl>guanine 
• 94426-73-0 9-<4-(benzyloxy)-2-hydroxybutyl>guanine 
• 94426-78-5 9-<4-(benzyloxy)-2-oxobutyl>adenine 
• 94426-74-1 9-<4-(benzyloxy)-2-hydroxybutyl>adenine 
• 94426-75-2 1-<4-(benzyloxy)-2-hydroxybutyl>uracil 
• 94426-76-3 1-<4-(benzyloxy)-2-hydroxybutyl>thymine 
• 94426-79-6 1-<4-benzyloxy)-2-oxobutyl>uracil 
• 94426-80-9 1-<4-(benzyloxy)-2-oxobutyl>thymine 
• 94426-72-9 2-(2-(benzyloxy)ethyl)oxirane 

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