162090-27-9

Upstream product

• 4860-82-6 2,3-anhydro-α-D-ribofuranoside de methyle 
• 162090-15-5 methyl 3-O-(t-butyldimethylsilyl)-2-deoxy-5-O-(1-naphthoyl)-2-C-(2-propenyl)-α-D-arabinofuranoside 
• 162090-11-1 methyl 2-deoxy-5-O-(1-naphthoyl)-2-C-(2-propenyl)-α-D-arabinofuranoside 
• 128790-83-0 methyl 2-deoxy-2-C-(2-propenyl)-α-D-arabinofuranoside 
• 86-55-5 1-naphthalenecarboxylic acid 
• 98-59-9 p-toluenesulfonyl chloride 
• 162090-17-7 methyl 3-O-(t-butyldimethylsilyl)-2-deoxy-2-C-(3-hydroxypropyl)-5-O-(1-naphthoyl)-α-D-arabinofuranoside 

Relevant academic research and scientific papers

Reaction of 2-deoxy-2-C-(3-bromoacetoxypropyl)-α-D-arabinofuranosides with oligonucleotide

Reaction of methyl 2-deoxy-2-C-(3-bromoacetoxypropyl)-α-D- arabinofuranosides, prepared from methyl 2,3-anhydro-α-D-ribofuranoside, with oligodeoxyribonucleotide (21mer) in acetonitrile-H2O (pH 7) and subsequent treatment with piperidine resulted in the cleavage of the nucleotide chain at the position G, A, and C.