55639-83-3

Upstream product

• 37112-31-5 levoglucosenone 
• 100-51-6 benzyl alcohol 
• 102719-10-8 1,6-anhydro-4-O-benzyl-3-deoxy-β-D-erythro-hexopyranos-2-ulose 

Downstream Products

• 171001-80-2 methyl 4-O-benzyl-6-bromo-3,6-deoxy-β-D-erythro-hexopyranoside 
• 171001-83-5 (1R,2R,4R,5S,7R)-2-methoxy-1-methoxycarbonylmethyl-4-methyl-7-phenyl-3,6-dioxabicyclo<3.2.1>octane 
• 171001-81-3 methyl 4-O-benzyl-6-bromo-3,6-deoxy-2-methoxycarbonylmethylene-β-D-erythro-hexopyranoside 
• 102719-15-3 2-O-acetyl-1,6-anhydro-3-deoxy-β-D-ribo-hexopyranose 
• 102719-16-4 Acetic acid (1R,4R,5R)-2-oxo-6,8-dioxa-bicyclo[3.2.1]oct-4-yl ester 
• 33647-85-7 isolevoglucosenone 
• 102719-13-1 2-O-acetyl-1,6-anhydro-4-O-benzyl-3-deoxy-β-D-ribo-hexopyranose 

Relevant academic research and scientific papers

Preparation of the diastereomerically pure 2S-hydroxy derivative of dihydrolevoglucosenone (cyrene)

Diastereomerically pure levoglucosenone alcohol, synthesized from levoglucosenone, upon hydrogenation on Raney Ni or Pd/BaSO4 undergoes epimerization at C2 atom caused by formation of cyrene by-product and its subsequent non-specific

Synthesis of α-bromoisolevoglucosenone and its cyclopenta annulation

4,4-Dimethyl-3-nitro-10,11-dioxatricyclo[6.2.1.02,6]undec-5-en-7-one possessing a bicyclic iridoid skeleton was synthesized in two steps from isolevoglucosenone which was obtained in turn from levoglucosenone through 4-benzyloxy-2-tosyloxy deri

SYNTHESIS AND THERMAL CHEMISTRY OF ISOLEVOGLUCOSENONE

Isolevoglucosenone (1,6-anhydro-2,3-dideoxy-β-D-glycero-hex-2-enopyranos-4-ulose, 3) has been synthesized from levoglucosenone (2) in six steps.Thus, 1,6-anhydro-4-O-benzyl-3-deoxy-β-D-erythro-hexopyranos-2-ulose, obtained by Michael addition of benzyl al