90626-63-4

Upstream product

• 1779-49-3 Methyltriphenylphosphonium bromide 
• 90626-64-5 2D-(2,3,6/4,5)-6-O-Benzyl-2,3:4,5-di-O-isopropyliden-2,3,4,5,6-pentahydroxycyclohexanon 
• 65533-41-7 1L-4-O-Benzyl-1,2:5,6-di-O-isopropyliden-chiro-inosit 
• 90694-04-5 1L-1,2:3,4:5,6-tri-O-isopropylidene-chiro-inositol 
• 65556-81-2 1L-1,2:5,6-di-O-isopropylidene-chiro-inositol 

Downstream Products

• 90626-65-6 1L-4-O-Benzyl-3-desoxy-3-C-hydroxymethyl-1,2:5,6-di-O-isopropyliden-allo-inosit 
• 52079-86-4 (1R)-(+)-(1,2,3/4,5)-2,3,4,5-tetrahydroxycyclohexane-1-methanol penta-acetate 
• 52079-85-3 (1R)-(+)-(1,2,3/4,5)-2,3,4,5-tetrahydroxycyclohexane-1-methanol 
• 90626-66-7 1L-4-O-Benzyl-3-desoxy-1,2:5,6-di-O-isopropyliden-3-C-<(2-methoxyethoxy)methoxymethyl>-allo-inosit 
• 90652-13-4 1L-3-C-Acetoxymethyl-4-O-benzyl-3-desoxy-1,2:5,6-di-O-isopropyliden-allo-inosit 

Relevant academic research and scientific papers

Cyclitol Reactions, X. - Synthesis of Enantiomerically Pure Pseudo-α-D-galactopyranose and Pseudo-β-D-mannopyranose

The L-chiro-inositol 2, prepared from quebrachitol, is transferred, via 5, into the inosose 7.Wittig reaction of 7 and subsequent hydroboration followed by oxidation leads to the hydroxymethyl branched-chain derivative 8.From this, via 11, the S-methyl di