80339-59-9

Upstream product

• 98-88-4 benzoyl chloride 
• 51255-17-5 1-O-methyl-2-deoxy-D-ribofuranoside 
• 533-67-5 2-deoxy-D-ribose 
• 51255-18-6 1-O-methyl-β-2-deoxy-D-erythro-pentofuranose 
• 533-67-5 2-Deoxy-D-ribose 
• 30591-84-5 methyl 3,5-di-O-benzoyl-L-arabinofuranoside 
• 51885-64-4 1,2-O-isopropylidene-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 
• 103763-12-8 5-O-tert-butyldiphenylsilyl-α,β-L-arabinofuranose 
• 6893-72-7 5-O-benzoyl-1,2-O-isopropylidene-β-L-arabinofuranose 
• 3080-31-7 3,5-di-O-benzoyl-1,2-O-isopropylidene-β-L-arabinofuranose 
• 51255-17-5 (2S,3R)-2-Hydroxymethyl-5-methoxy-tetrahydro-furan-3-ol 
• 43179-48-2 L-arabinose di(ethylthio)acetal 
• 5328-37-0 L-arabinose 

Downstream Products

• 77180-98-4 1-(2-deoxy-3,5-di-O-benzoyl-β-L-erythro-pentofuranosyl)-5-fluorouracil 
• 137172-45-3 1-O-acetyl-3,5-di-O-benzoyl-2-deoxy-α-L-erythro-pentofuranoside 
• 137172-46-4 1-O-acetyl-3,5-di-O-benzoyl-2-deoxy-β-L-erythro-pentofuranoside 
• 21740-23-8 3,5-O-bis(4-chlorobenzoyl)-2-deoxy-α-D-ribofuranosyl chloride 
• 95041-53-5 C₁₉H₁₈O₆ 

Relevant academic research and scientific papers

Iron-Catalyzed Radical Cleavage/C?C Bond Formation of Acetal-Derived Alkylsilyl Peroxides

A novel radical-based approach for the iron-catalyzed selective cleavage of acetal-derived alkylsilyl peroxides, followed by the formation of a carbon–carbon bond is reported. The reaction proceeds under mild reaction conditions and exhibits a broad substrate scope with respect to the acetal moiety and the carbon electrophile. Mechanistic studies suggest that the present reaction proceeds through a free-radical process involving carbon radicals generated by the homolytic cleavage of a carbon–carbon bond within the acetal moiety. A synthetic application of this method to sugar-derived alkylsilyl peroxides is also described.

A parallel synthesis approach towards a family of C-nucleosides

A synthetic route was devised for a sugar based α-chloroketone, which was subsequently used to generate a family of C-nucleosides via parallel synthetic methodology.

Preparation of new acylated derivatives of L-arabinofuranose and 2-deoxy-L-erythro-pentofuranose as precursors for the synthesis of L-pentofuranosyl nucleosides

1,2-Di-O-acetyl-3,5-di-O-benzoyl-L-rabinofuranose and 1-O-acetyl-3,5-di-O-benzoyl-2-deoxy-L-erythro-pentofuranose have been synthesised from L-rabinose for use in the preparation of L-pentofuranosyl nucleosides. 1,2-Di-O-acetyl-3,5-di-O-benzoyl-L-arabinof

BAKER'S YEAST MEDIATED PREPARATION OF CARBOHYDRATE-LIKE CHIRAL SYNTHONS

Baker's yeast mediated reduction of the α-acetoxy ketones (1)-(3) proceeds with high enantio- and stereoselectivity to give the anti carbinols (4)-(6), easily converted into the masked chiral deoxy sugars (12)-(14), from which D- and L-deoxysugars have be

5(S), 6(R)-5, 7-DIBENZOYLOXY-6-HYDROXYHEPTANOATE ESTER : IMPROVED SYNTHESIS OF A LEUKOTRIENE INTERMEDIATE

The title compound, a key intermediate in the synthesis of leukotriene A4, was prepared by a convenient procedure from 2-deoxy-D-ribose.