136522-41-3

Upstream product

• 100-39-0 benzyl bromide 
• 97-30-3 methyl-alpha-D-glucopyranoside 
• 136471-95-9 methyl 3,4-bis(O-methoxymethyl)-2,6-bis-α-D-glucopyranoside 
• 136471-98-2 (2S,3R,4S)-4-Benzyloxy-5-hydroxy-2,3-bis-methoxymethoxy-cyclohexanone 
• 136471-99-3 <2S-(2α,3β,4α)>-4-(Benzyloxy)-2,3-bis(methoxymethoxy)-5-cyclohexen-1-one 
• 171815-12-6 <1S-(1α,2β,3α,4β)>-4-(Benzyloxy)-2,3-bis(methoxymethoxy)-5-cyclohexen-1-ol 
• 160835-77-8 methyl 6-deoxy-3,4-bis(O-methoxymethyl)-α-D-xylo-hex-5-enopyranoside 
• 54497-89-1 methyl 2,6-bis-α-D-glucopyranoside 
• 136472-00-9 1D-(1,3/2,4)-1,4-di-O-benzyl-2,3-bis(O-methoxymethyl)-5-cyclohexene-1,2,3,4-tetrol 

Downstream Products

• 136472-01-0 1D-2,3,6-tri-O-benzyl-1,4,5-tris(O-methoxymethyl)-1,2,3,5/4,6-cyclohexanehexol 
• 160835-78-9 1D-3,6-di-O-benzyl-1,4,5-tris(O-methoxymethyl)-1,2,3,5/4,6-cyclohexanehexol 
• 104873-76-9 2,3,6-tris-O-(phenylmethyl)-D-myo-inositol 

Relevant academic research and scientific papers

Syntheses of Optically Active 2,3,6-Tri-O-benzyl-D-myo-inositol, Laminitol, and Mytilitol from D-Glucose

2,3,6-Tri-O-benzyl-D-myo-inositol, which is a key intermediate of D-inositol 1,4,5-triphosphate, was synthesized from D-glucose without performing any optical resolution by utilizing C2 symmetry.Laminitol and mytilitol were also synthesized from D-glucose

Synthesis of Optically Active 2,3,6-Tri-O-benzyl-D-myo-inositol from D-Glucose

The title compound was synthesized from D-glucose as a key intermediate of D-Inositol-1,4,5-triphosphate synthesis without doing any optical resolution by utilizing C2 symmetry.