114218-30-3

Upstream product

• 114218-19-8 1D-3-O-allyl-1,2,4-tri-O-benzyl-5,6-O-isopropylidene-myo-inositol 
• 114218-16-5 1L-(-)-1-O-allyl-2,3,6-tri-O-benzyl-myo-inositol 
• 111446-91-4 (+/-)-1,2,4-tri-O-benzyl-5,6-O-isopropylidene-myo-inositol 
• 114218-18-7 (-)-ω-camphanate of 1D-1,2,4-tri-O-benzyl-5,6-O-isopropylidene-myo-inositol 
• 181272-70-8 C₃₁H₄₄O₉ 
• 181489-61-2 (-)-1,2:4,5-di-O-cyclohexylidene-3-O-allyl-myo-inositol 
• 129879-48-7 (+/-)-1,2:4,5-di-O-cyclohexylidene-3-O-allyl-myo-inositol 
• 100-39-0 benzyl bromide 
• 114218-29-0 1L-1-O-allyl-2,3,4,5,6-penta-O-benzyl-myo-inositol 
• 114297-90-4 1D-1,2,4-tri-O-benzyl-5,6-O-isopropylidene-myo-inositol 

Downstream Products

• 26277-05-4 1,2,4,5,6-penta-O-benzyl-sn-myo-inositol 

Relevant academic research and scientific papers

1D- and 1L-1,2:4,5-di-O-cyclohexylidene-3-O-allyl-myo-inositols: Complementary versatile new starting materials for syntheses in the 1D-myo- inositol series

The preparation and proof of absolute configuration as 1D- and 1L- respectively are presented for (-)and (+)-1,2:4,5-di-O-cyclohexylidene-3-O- allyl-myo-inositol, two versatile complementary materials equally suitable for syntheses in the 1D-myo-inositol

The Allyl Group for Protection in Carbohydrate Chemistry. Part 20. Synthesis of 1L-1-O-Methyl-myo-inositol by Resolution of (+/-)-1,2,4-Tri-O-benzyl-myo-inositol

Racemic 1,2,4-tri-O-benzyl-myo-inositol was prepared by two new routes from (+/-)-1,4-di-O-benzyl-5,6-O-isopropylidine-myo-inositol, one route involving the crystalline intermediate (+/-)-1-O-allyl-3,6-di-O-benzyl-4,5-O-isopropylidine-myo-inositol.Oxidati