81076-89-3

Upstream product

• 76690-23-8 (1S,2S,3S,4R,5R)-2,4-Dimethyl-6,8-dioxabicyclo<3.2.1>octan-3-ol 
• 100-39-0 benzyl bromide 
• 81076-81-5 1,6-anhydro-3-O-benzyl-2,4-dideoxy-2-C-methyl-4-methylene-β-D-xylohexopyranose 
• 81076-77-9 1,6-anhydro-2-desoxy-2,4-di-C-methyl-3-O-benzyl-β-D-galactopyranose 
• 76706-48-4 1,6-anhydro-2-desoxy-2,4-di-C-methyl-β-D-galactopyranose 
• 100-44-7 benzyl chloride 
• 85433-11-0 (1S,2S,3S,4R,5R)-2-methyl-4-<(p-toluenesulfonyl)-oxy>-6,8-dioxabicyclo<3.2.1>octan-3-ol 
• 85433-12-1 (1S,2S,3S,4S,5R)-2-Methyl-3,4-epoxy-6,8-dioxabicyclo<3.2.1>octan-3-ol 
• 81076-80-4 1,6-anhydro-2-desoxy-2,4-di-C-methyl-3-O-benzyl-4-O-mesyl-β-D-galactopyranose 

Downstream Products

• 81076-90-6 ((2S,3S,4S,5R)-4-Benzyloxy-6-methoxy-3,5-dimethyl-tetrahydro-pyran-2-yl)-methanol 
• 101536-34-9 methyl-α-3-O-benzyl-2,4-didesoxy-2,4-di-C-methyl-D-glucopyranoside 
• 110104-48-8 (2S,3R,4S,5R)-4-Benzyloxy-5-[1,3]dithian-2-yl-3-methyl-hexane-1,2-diol 
• 110104-49-9 (2R,3S,4R)-3-Benzyloxy-4-[1,3]dithian-2-yl-2-methyl-pentan-1-ol 
• 101628-76-6 methyl-α-3-O-benzyl-2,4,6-tridesoxy-2,4-di-C-methyl-D-glucopyranoside 

Relevant academic research and scientific papers

THE OXIRANE RING OPENINGS OF THE DIANHYDRO SUGAR WITH HIGH REGIOSELETIVITY AND ITS USE IN PREPARATION OF TWO CHIRAL SEGMENTS OF 6-DEOXYERYTHRONOLIDE B

The oxirane ring of the dianhydro sugar 2 obtained from levoglucosan (1,6-anhydro-β-D-glucose) is opened regioselectively with organometallic carbon nucleophiles and its application to an asymmetric synthesis of the C1-C5 segment 9 t

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.