17230-38-5

Upstream product

• 642-38-6 quebrachitol 
• 17230-37-4 1L-5,6-O-Isopropyliden-2-O-methyl-chiro-inosit 
• 108-24-7 acetic anhydride 
• 80971-01-3 1L-1,3,4-Tri-O-acetyl-5,6-O-isopropyliden-2-O-methyl-chiro-inosit 

Downstream Products

• 134235-66-8 1D-1,2,3,5-tetra-O-acetyl-6-azido-6-deoxy-4-O-methyl-muco-inositol 
• 134235-58-8 1L-1,3,4,5-tetra-O-acetyl-6-azido-6-deoxy-2-O-methyl-chiro-inositol 
• 57784-02-8 1L-1-acetamido-2,3,4,5-tetra-O-acetyl-1-deoxy-6-O-methyl-scyllo-inositol 
• 134235-67-9 1L-3-acetamido-1,2,4,6-tetra-O-acetyl-3-deoxy-5-O-methyl-muco-inositol 
• 134235-59-9 1L-1-acetamido-2,3,4,6-tetra-O-acetyl-2-deoxy-5-O-methyl-chiro-inositol 
• 134159-84-5 1D-2,4-diacetamido-1,3,5-tri-O-acetyl-2,4-dideoxy-6-O-methyl-chiro-inositol 
• 134159-85-6 1D-1,2,3-tri-O-acetyl-5,6-diazido-5,6-dideoxy-4-O-methyl-chiro-inositol 
• 134159-86-7 1D-1,2-diacetamido-4,5,6-tri-O-acetyl-1,2-dideoxy-3-O-methyl-chiro-inositol 
• 80980-00-3 1L-1,2-Anhydro-4,5-di-O-acetyl-3-O-methyl-6-O-p-tolylsulfonyl-myo-inosit 
• 80979-99-3 1L-(1,2,4/3)-1,3,4-Tri-O-acetyl-2-O-methyl-tetrahydroxy-5-cyclohexen 
• 18438-18-1 2-O-Methyl-5-O-tosyl-(-)-inosit 
• 18391-44-1 1L-1,3,4-Tri-O-acetyl-2-O-methyl-5,6-di-O-p-tolylsulfonyl-chiro-inosit 
• 17230-40-9 1L-1,3,4-tri-O-acetyl-2-O-methyl-5-O-p-tolylsulfonyl-chiro-inositol 
• 134159-71-0 1L-1,3,4-tri-O-acetyl-2-O-methyl-5,6-di-O-methylsulfonyl-chiro-inositol 

Relevant academic research and scientific papers

Synthesis of several optically active O-methyl-inosamines and -inosadiamines from L-quebrachitol

A series of p-toluenesulfonic and methanesulfonic esters of L-quebrachitol have been prepared starting from the di-O-isopropylidene derivative of the cyclitol.Nucleophilic displacement of these sulfonates with azide ion in 2-methoxyethanol produced the az

Cyclitol Reactions, V. - Synthesis of Enantiomerically Pure Valienamine from Quebrachitol

An enantioselective synthesis of Valienamine (86) from quebrachitol (L-2O-methyl-chiro-inositol) (1) is described.Valienamine (86) is an unsaturated branched-chain aminocyclitol found in the central structural unit of the antidiabetic drug acarbose.Techniques for the introduction of side chains, azido groups, and double bonds into inositol systems are investigated.The methods developed in this connection are applied in the synthesis of valienamine.