72076-10-9

Upstream product

• 67-56-1 methanol 
• 13007-49-3 methyl 3,6-di-O-benzoyl-4-deoxy-α-D-glycero-hex-3-enopyranosid-2-ulose 
• 68325-67-7 Methyl 2,4,6-Tri-O-benzoyl-α-D-ribo-hexopyranosid-3-uloside 
• 72076-13-2 (+)-(2R,3R)-3,5-Bis(benzoyloxy)-2-(benzoyloxymethyl)-2,3-dihydro-4H-pyran-4-one 
• 2092-61-7 3-oxo-β-D-glucose 
• 68366-59-6 (2R,4aR,6S,7R,8aR)-6-methoxy-8-oxo-2-phenyl-7-phenylcarbonyloxyperhydropyrano[3,2-d][1,3]dioxine 
• 2847-00-9 1,2:5,6-di-O-isopropylidene-α-D-hexofuran-3-ulose 

Relevant academic research and scientific papers

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

ANOMERIC STEREOCONTROL IN ADDITION REACTIONS TO HEXOSE-DERIVED DIHYDROPYRANONES

The outcome of base-catalysed O- and C-nucleophile additions to the carbonyl group of benzoylated 4-deoxy-D-glycero-hex-3-enopyranosid-2-ulose (1) depends on the conditions used.With methanol / sodium iodide, methanol / sodium methoxide (traces), or methy