51785-70-7

Upstream product

• 51255-17-5 (2S,3R)-2-Hydroxymethyl-5-methoxy-tetrahydro-furan-3-ol 
• 98-88-4 benzoyl chloride 
• 51255-17-5 1-O-methyl-2-deoxy-D-ribofuranoside 
• 533-67-5 2-deoxy-D-ribose 
• 30591-84-5 methyl 3,5-di-O-benzoyl-L-arabinofuranoside 
• 3080-31-7 3,5-di-O-benzoyl-1,2-O-isopropylidene-β-L-arabinofuranose 
• 6893-72-7 5-O-benzoyl-1,2-O-isopropylidene-β-L-arabinofuranose 
• 5328-37-0 L-arabinose 
• 43179-48-2 L-arabinose di(ethylthio)acetal 
• 77772-43-1 5-O-benzoyl-L-arabinose diethyl dithioacetal 
• 103763-12-8 5-O-tert-butyldiphenylsilyl-α,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 
• 51885-64-4 1,2-O-isopropylidene-β-L-arabinofuranose 

Downstream Products

• 95041-53-5 3,5-Di-O-benzoyl-2-desoxy-D-ribose 
• 95041-53-5 C₁₉H₁₈O₆ 
• 55734-51-5 1,4-anhydro-2-deoxy-3,5-di-O-benzoyl-D-erythro-pent-1-enitol 
• 145417-01-2 2-pyridyl 3,5-di-O-benzoyl-2-deoxy-1-thio-α,β-D-ribofuranoside 
• 140186-56-7 methyl 2,3-O-isopropylidene-5-O-(3,5-di-O-benzoyl-2-deoxy-α-D-ribofuranosyl)-α-D-ribofuranoside 
• 140186-58-9 1,2:5,6-di-O-isopropylidene-3-O-(3,5-di-O-benzoyl-2-deoxy-α-D-ribofuranosyl)-α-D-glucofuranoside 
• 140186-57-8 1,2:3,4-di-O-isopropylidene-5-O-(3,5-di-O-benzoyl-2-deoxy-α-D-ribofuranosyl)-α-D-galactopyranoside 
• 140186-59-0 methyl 2,3-di-O-benzyl-6-O-(3,5-di-O-benzoyl-2-deoxy-α-D-ribofuranosyl)-α-D-glucopyranoside 
• 80311-45-1 C₂₃H₂₄O₇ 
• 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 
• 77180-98-4 1-(2-deoxy-3,5-di-O-benzoyl-β-L-erythro-pentofuranosyl)-5-fluorouracil 

Relevant academic research and scientific papers

Visible-Light Photocatalysis Employing Dye-Sensitized Semiconductor: Selective Aerobic Oxidation of Benzyl Ethers

The aerobic oxidation is an attractive approach toward environmentally benign synthesis of fine chemicals. In addition, dye-sensitized semiconductors are underdeveloped photocatalysts for selective organic synthesis. With the aid of catalytic eosin Y-sensitized titanium dioxide, we have developed efficient aerobic photooxidation of benzyl ethers to benzoates, featuring low cost, high atom economy, broad substrate scope, and user-friendly setup. Furthermore, preliminary mechanistic studies established that the reaction pathway likely entails a photoinduced, radical-based two-step process via an isolable peroxide intermediate.

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.