85271-59-6

Upstream product

• 100-44-7 benzyl chloride 
• 498-07-7 levoglucosan 
• 97321-52-3 C₁₅H₁₈O₄ 
• 100-39-0 benzyl bromide 
• 81099-73-2 methyl-2-desoxy-2,4-di-C-methyl-3,4-di-O-benzyl-α-D-glucopyranoside 
• 85317-33-5 methyl 2-desoxy-2,4-di-C-methyl-3,4-di-O-benzyl-α,β-D-glucopyranoside 
• 81076-80-4 1,6-anhydro-2-desoxy-2,4-di-C-methyl-3-O-benzyl-4-O-mesyl-β-D-galactopyranose 
• 81076-82-6 1,6-anhydro-2-desoxy-2,4-di-C-methyl-3-O-benzyl-4-O-mesyl-β-D-glucopyranose 
• 81076-83-7 1,6-anhydro-2-desoxy-2,4-di-C-methyl-3,4-di-O-benzyl-β-D-glucopyranose 
• 91510-67-7 1,6-anhydro-2-desoxy-2-C-methyl-3-O-benzyl-4-O-allyl-β-D-glucopyranose 
• 91510-66-6 1,6-anhydro-2-desoxy-2-C-methyl-3-O-benzyl-β-D-xylohexapyranos-4-ylose 
• 91510-65-5 1,6-anhydro-2-desoxy-2-C-methyl-3-O-benzyl-β-D-glucopyranose 
• 76706-48-4 1,6-anhydro-2-desoxy-2,4-di-C-methyl-β-D-galactopyranose 
• 91510-63-3 4-O-Allyl-1,6:2,3-dianhydro-β-D-mannopyranose 

Downstream Products

• 81099-74-3 methyl-2,6,7-tridesoxy-2,4-di-C-methyl-3,4-di-O-benzyl-α-D-glucoheptapyranoside 

Relevant academic research and scientific papers

SYNTHESIS OF MACROLIDE ANTIBIOTICS. 2. SYNTHESIS OF THE C9-C13 SEGMENTS OF ERYTHRONOLIDES A, B AND OLEANDONOLIDE

The C9-C13 segments of some 14-membered macrolide antibiotics have been synthesized from levoglucosan.