168103-01-3

Upstream product

• 100-39-0 benzyl bromide 
• 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 
• 100-44-7 benzyl chloride 

Downstream Products

• 168102-96-3 methyl 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-galacto-heptofuranuronate 
• 168102-97-4 methyl 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-β-L-altro-heptofuranuronate 
• 168103-02-4 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-galacto-heptofuranose 
• 168103-03-5 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-β-L-altro-heptofuranose 
• 65462-15-9 3-O-benzyl-1,2-O-isopropylidene-β-L-arabino-pentodialdo-1,4-furanose 
• 883740-55-4 6-N-benzoyl-9-[2-O-tert-butyldimethylsilyl-5-O-(4,4'-dimethoxytrityl)-α-L-ribofuranosyl]adenine 
• 883740-53-2 6-N-benzoyl-9-[5-O-(4,4'-dimethoxytrityl)-α-L-ribofuranosyl]adenine 
• 525596-24-1 9-(2-O-acetyl-5-O-benzoyl-3-O-benzyl-α-L-ribofuranosyl)-6-N-benzoyladenine 
• 525596-22-9 9-(2-O-acetyl-5-O-benzoyl-3-O-benzyl-α-L-arabinofuranosyl)-6-N-benzoyladenine 
• 525596-23-0 6-N-benzoyl-9-(5-O-benzoyl-3-O-benzyl-α-L-arabinofuranosyl)adenine 
• 883740-49-6 N-[9-(4-benzyloxy-3-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-9H-purin-6-yl]-benzamide 
• 883740-51-0 6-N-benzoyl-9-(α-L-ribofuranosyl)adenine 
• 525596-21-8 1,2-di-O-acetyl-5-O-benzoyl-3-O-benzyl-L-arabinofuranose 

Relevant academic research and scientific papers

Total Synthesis, Configuration Assignment, and Cytotoxic Activity Evaluation of Protulactone A

The first total synthesis and absolute configuration assignment of protulactone A (1) has been achieved. Four stereoisomers, 1a, ent-1a, 1b, and ent-1b, of this natural polyketide were prepared by chiral pool synthesis starting from l- and d-arabinose, re

Synthesis of tri- and tetrasaccharide glycosides of (4S)-4-hydroxy-d-proline relevant to the cell wall O-glycans of green alga Chlamydomonas reinhardtii

The synthesis of tri- and tetrasaccharide glycosides of (4S)-4-hydroxy-d-proline 1 and 2 with unusual glycan motifs has been achieved efficiently. The assembly of the synthetically challenging 1,2-cis linked arabino- and galactofuranoside frameworks withi

Convenient conversion of wheat hemicelluloses pentoses (d-xylose and l-arabinose) into a common intermediate

The transformation of d-xylose and l-arabinose, the two major components of wheat straw and bran, into a unique multifunctional, optically pure, five-carbon synthon has been achieved. The synthetic sequence requires three steps: suitable protection of the

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

The Raction of Acetyliron 5-C5H5)Fe(CO)(PPh3)(COCH3)> with Sugar Aldehydes. New Synthesis of Deoxysugars

Aldol reactions of sugar aldehydes (5-13) with enolate 2 of racemic and both enantiomeric forms of acetyliron were investigated.The steric course of reactions depended strongly on the counterions used.High stereocontrol was achieved with the following cat