58262-15-0

Upstream product

• 79292-17-4 methyl 2,6-anhydro-D-glycero-L-gluco-heptonate 
• 78393-35-8 3,4,5,7-Tetra-O-acetyl-2,6-anhydro-D-glycero-L-gluco-heptonamide 
• 656224-04-3 dimethyl 3,4,5-tri-O-benzoyl-2,6-anhydro-D-glycero-L-gluco-heptarate 
• 656224-06-5 dimethyl 2,6-anhydro-5-O-mesyl-D-glycero-L-gluco-heptarate 
• 656224-02-1 dimethyl 2,6-anhydro-D-glycero-L-gluco-heptarate 
• 14125-78-1 2,3,4,6-tetra-O-acetyl-1,5-anhydro-D-lyxo-hex-1-enitol 
• 656224-05-4 dimethyl 2,6-anhydro-3,4-di-O-benzoyl-5-O-mesyl-D-glycero-L-gluco-heptarate 

Relevant academic research and scientific papers

(-)-Daucic Acid: Revision of Configuration, Synthesis, and Biosynthetic Implications

The synthesis of dihydropyrans with the D-xylo (1), D-ribo, L-arabino, and D-lyxo (2) configuration by one-carbon-atom homologation of D-mannose or D-galactose, terminal oxidation, and directed β elimination revealed (-)-daucic acid isolated from carrots

(-)-Daucic acid: Proof of D-lyxo configuration, synthesis of its D-ribo, D-xylo, L-arabino and L-lyxo analogs, and biosynthetic implications

The dimethyl esters of the 2,6-anhydro-3-deoxy-hept-2-enaric acids with D-xylo, D-lyxo, L-arabino, L-lyxo- and D-ribo-configuration were synthesized from D-galactose and D-mannose, respectively, and further characterized by their di-O-acetyl and di-O-benz