1334376-84-9

Upstream product

• 100-39-0 benzyl bromide 
• 1218932-89-8 S-methyl O-((1R,3r,5S,6R,7s,8S,9r)-6,8,9-tris(benzyloxy)-3-phenyl-2,4-dioxabicyclo[3.3.1]nonan-7-yl) carbonodithioate 
• 1335029-85-0 S-methyl O-((1R,3r,5S,6R,7r,8S,9r)-6,8,9-tris(benzyloxy)-3-phenyl-2,4-dioxabicyclo[3.3.1]nonan-7-yl) carbonodithioate 
• 1218787-82-6 2,4,6-tri-O-benzyl-1,3-O-benzylidene-5-O-[(methylthio)thiocarbonyl]myo-inositol 
• 1335029-87-2 2,4,6-tri-O-benzyl-1,3-O-benzylidene-5-O-[(methylthio)thiocarbonyl]neo-inositol 
• 940000-68-0 6,8,9-tris-benzyloxy-3-phenyl-2,4-dioxa-bicyclo[3.3.1]nonan-7-ol 

Relevant academic research and scientific papers

Thermal epimerization of inositol 1,3-benzylidene acetals in the molten state

1,3-O-Benzylidene-2,4,5,6-tetra-O-substituted-myo-inositol derivatives obtained by the DIBAL-H reduction of the corresponding myo-inositol 1,3,5-orthobenzoate derivatives undergo epimerization at the acetal carbon on heating, in the molten state, just abo