72076-13-2

Upstream product

• 98-88-4 benzoyl chloride 
• 158715-81-2 (+)-(2R,3R)-3,5-dihydroxy-2-hydroxymethyl-2,3-dihydro-4H-pyran-4-one 
• 1883-12-1 3-ketosucrose 
• 2847-00-9 1,2:5,6-di-O-isopropylidene-α-D-hexofuran-3-ulose 

Downstream Products

• 72076-10-9 (-)-(2S,3S)-3-(Benzoyloxy)-2,3-dihydro-2,3-dimethoxy-6-methyl-4H-pyran-4-one 
• 72076-12-1 (2R,3R)-3-(Benzoyloxy)-2,3-dihydro-2,3-dimethoxy-6-methyl-4H-pyran-4-one 
• 68325-67-7 Methyl 2,4,6-Tri-O-benzoyl-α-D-ribo-hexopyranosid-3-uloside 
• 122409-65-8 (-)-(2R,6S)-4-(Benzoyloxy)-6-(benzoyloxymethyl)-2-methyl-2H-pyran-3(6H)-one 
• 122409-67-0 (+)-(4aS,8aR)-8a-(Benzoyloxy)-6-methyl-2,3,4a,8a-tetrahydro-8H-pyrano<2,3-b>-1,4-dioxin-8-one 
• 122409-63-6 (+)-(2R,3S)-3,5-Bis(benzoyloxy)-2-(benzoyloxymethyl)-3,4-dihydro-4-methylene-2H-pyrane 
• 122424-07-1 3,4,6-Tri-O-benzoyl-1,2-O-isopropylidene-β-D-mannopyranose 
• 122409-66-9 3,4,6-Tri-O-benzoyl-1,2-O-isopropylidene-β-D-erythro-hex-2-enopyranose 
• 122409-64-7 (2,4,6-Tri-O-benzoyl-β-D-ribo-hexopyranos-3-ulosyl)acetophenon 

Relevant academic research and scientific papers

Regioselective synthesis of new sucrose derivatives via 3-ketosucrose

3-Ketosucrose (α-D-ribo-hexopyranosyl-3-ulose-β-D-fructofuranoside), obtained from sucrose via microbial oxidation with Agrobacterium tumefaciens, was shown to be an appropriate and versatile synthon for regioselective syntheses. Condensation with hydroxy

Enantiomerically Pure Building Blocks from Sugars, 10 2,3-Dihydropyranones with Contiguous Chiral Centers: Practical Routes for Their Aquisition and Evaluation of their Reaction Potential

A practical, large-scale adaptable four-step procedure has been developed for the conversion of D-glucose into pyranoid enediolone esters with (R,R)-configuration in contiguous chiral centers, involving hydrolysis of the readily accessible bis-acetonide o