110237-79-1

Upstream product

• 1333476-18-8 methyl 5-O-benzoyl-β-L-arabinoside 
• 6893-72-7 5-O-benzoyl-1,2-O-isopropylidene-β-L-arabinofuranose 
• 100-39-0 benzyl bromide 
• 98-88-4 benzoyl chloride 
• 3795-69-5 methyl β-L-arabinofuranoside 
• 957766-91-5 3-O-benzyl-1,2-O-isopropylidene-5-O-triphenylmethyl-β-L-arabinofuranose 
• 168103-01-3 3-O-benzyl-1,2-O-isopropylidene-5-O-(tert-butyldiphenylsilyl)-β-L-arabinofuranose 
• 103763-14-0 (3aR,5S,6S,6aR)-5-{[(tert-butyldiphenylsilyl)oxy]methyl}-2,2-dimethyltetrahydro-2H-furo[2,3-d][1,3]dioxol-6-ol 
• 68354-70-1 3-O-benzyl-1,2-O-isopropylidene-β-L-arabinofuranose 

Downstream Products

• 1333476-19-9 diethyl (5R)-(3-O-benzyl-1,2-O-isopropylidene-β-L-arabinofuranos-5-C-yl)phosphonate 
• 1333476-20-2 diethyl (5S)-(3-O-benzyl-1,2-O-isopropylidene-β-L-arabinofuranos-5-C-yl)phosphonate 
• 68354-70-1 3-O-benzyl-1,2-O-isopropylidene-β-L-arabinofuranose 
• 65462-15-9 3-O-benzyl-1,2-O-isopropylidene-β-L-arabino-pentodialdo-1,4-furanose 
• 1611459-91-6 (4R,5R)-5-(benzyloxy)-4-[(1'R)-1'-isothiocyanatoallyl]-2,2-dimethyl-1,3-dioxane 
• 1611459-93-8 (4R,5R)-5-(benzyloxy)-4-[(1'S)-1'-isothiocyanatoallyl]-2,2-dimethyl-1,3-dioxane 

Relevant academic research and scientific papers

Total synthesis and antiproliferative/cytotoxic profiling of 2-epi-jaspine B

A straightforward access to 2-epi-jaspine B (4.HCl) has been developed. Key to the approach was the use of Overman rearrangement for the instalment of a stereocentre bearing a nitrogen atom. Subsequent rational execution of the stereoselective transformat

Tetrofuranose nucleoside phosphonic acids: Synthesis and properties

New isoelectronic, non-isosteric phosphonate analogues of nucleoside 5'-phosphates featuring the phosphorus moiety directly attached on the sugar ring in the C4' position are described. The analogues were synthesised by a nucleosidation reaction from tetr

Synthesis and RNA-selective hybridization of α-L-ribo- and β-D-lyxo-configured oligonucleotides

Three α-l-ribofuranosyl analogues of RNA nucleotides (α-l-RNA analogues) have been synthesized and incorporated into oligonucleotides using the phosphoramide approach on an automated DNA synthesizer. The 4′-C-hydroxymethyl-α-l-ribofuranosyl thymine monome