59556-69-3

Upstream product

• 54946-48-4 benzyl-β-D-ribofuranoside 
• 98-88-4 benzoyl chloride 
• 55797-81-4 O²,O³,O⁵-Tribenzoyl-D-ribose 
• 100-51-6 benzyl alcohol 
• 50-69-1 D-ribose 
• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 22860-91-9 2,3,5-tri-O-benzoyl-D-ribofuranosyl bromide 
• 69350-76-1 methyl 2,3,5-tri-O-benzoyl-αβ-D-ribofuranoside 
• 1824-96-0 methyl ribofuranoside 
• 66981-58-6 3,5-di-O-benzoyl-α-D-ribofuranoside-prop-2-ynyl-1,2-orthobenzoate 
• 1927-62-4 tetrahydro-2-(benzyloxy)-2H-pyran 

Downstream Products

• 93215-12-4 benzyl 5-O-benzoyl-β-D-ribofuranoside 
• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 93215-26-0 methyl -8-O-benzyl-4,5-O-carbonyl-3-deoxy-α-D-manno-2-octulopyranosid>onate 
• 93215-19-1 methyl -8-O-benzyl-4,5-O-carbonyl-3-deoxy-β-D-manno-2-octulopyranosid>onate 
• 93215-27-1 methyl -4,5-O-carbonyl-3-deoxy-α-D-manno-2-octulopyranosid>onate 
• 93215-20-4 methyl -4,5-O-carbonyl-3-deoxy-β-D-manno-2-octulopyranosid>onate 
• 93215-14-6 benzyl 5-O-benzoyl-3-O-benzyl-2-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranoside 
• 93215-18-0 methyl 3-O-acetyl-5-O-benzoyl-2-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranoside 
• 93215-17-9 1,3-di-O-acetyl-5-O-benzoyl-2-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-β-D-ribofuranose 
• 93245-42-2 3-O-acetyl-5-O-benzoyl-2-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-D-ribofuranosyl bromide 
• 93215-15-7 5-O-benzoyl-2-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-D-ribofuranose 
• 93549-35-0 5-O-benzoyl-3-O-benzyl-2-O-(p-nitrobenzoyl)-β-D-ribofuranoside 
• 93549-34-9 5-O-benzoyl-2-O-benzyl-3-O-(p-nitrobenzoyl)-β-D-ribofuranoside 
• 93245-41-1 benzyl 5-O-benzoyl-3-O-benzyl-β-D-ribofuranoside 

Relevant academic research and scientific papers

Gold(III)-catalyzed glycosidations for 1,2- trans and 1,2- cis furanosides

Stereoselective synthesis of furanosides is still a daunting task, unlike the pyranosides, for which several methods exist. Herein, a unified stereoselective strategy for the synthesis of 1,2-trans and 1,2-cis furanosides is revealed for seven out of eight possible isomers of pentoses. The identified protocol gives access to diastereoselective synthesis of α- and β-araf, ribf, lyxf, and α-xylf furanosides. 1,2-trans glycosides were synthesized by the use of propargyl 1,2-orthoesters under gold-catalyzed glycosidation conditions, and subsequently, they are converted into 1,2-cis glycosides through oxidation-reduction as the key functional group transformation. All the reactions are found to be fully diastereoselective, mild, and high yielding.

Synthesis of alkylcarbonate analogs of O-acetyl-ADP-ribose

The non-hydrolyzable alkylcarbonate analogs of O-acetyl-ADP-ribose have been synthesized from the phosphorylated ribose derivatives after coupling with AMP morpholidate promoted by mechanical grinding. The analogs were assessed for their ability to inhibi

Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf

(Chemical Equation Presented) A wide variety of p-tolyl thioriboside donors are examined for O-ribosylations of primary and secondary alcohols. p-Tolylsulfenyl trifluoromethanesulfonate (p-TolSOTf) is very effective in promoting O-ribosylations with p-tol

A One-pot Glycosylation of Tetrahydropyranyl (THP) Ether Intermediates

Tetrahydropyranyl (THP) derivatives of alcohols are converted in one-pot and in stereoselctive manner into the corresponding 1-O-alkyl-2,3,5-tri-O-benzoyl-β-D-ribofuranosides on treatment with 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose and trimethyls