6763-52-6

Upstream product

• 6763-54-8 1L-1,2:3,4-di-O-cyclohexylidene-5-O-methyl-6-O-(p-tolylsulfonyl)-chiro-inositol 
• 58769-23-6 1L-3,4,:5,6-di-O-isopropylidene-2-O-methyl-chiro-inositol 
• 98-59-9 p-toluenesulfonyl chloride 
• 4079-42-9 (+/-)-1,2,3,4,5-Penta-O-acetyl-6-O-tosyl-myo-inosit 
• 1122-84-5 1-ethoxycyclohexene 
• 6848-53-9 L-3,4:5.6-di-O-cyclohexylidene-2-O-methyl-(-)-chiro-inositol 
• 3006-56-2 1L-1,2:3,4-di-O-isopropylidene-5-O-methyl-6-O-p-tolylsulfonyl-chiro-inositol 

Downstream Products

• 52432-16-3 (+)-3-deoxy-3-azido-myo-inositol 
• 6090-98-8 (1R,2R,3R,4S)-5-cyclohexene-1,2,3,4-tetrol 
• 76139-17-8 1D-(1N,2,4/3)-1-Azido-2,3,4-tris(benzyloxy)-5-cyclohexen 
• 80178-02-5 1L-1,2-Anhydro-4-O-benzyl-myo-inosit 
• 80177-96-4 1L-5,6-O-Isopropyliden-1-O-tosyl-chiro-inosit 
• 80178-00-3 1L-4-O-Benzyl-1-O-tosyl-chiro-inosit 
• 80177-98-6 1L-4-O-Benzyl-2,3:5,6-di-O-isopropyliden-1-O-tosyl-chiro-inosit 
• 3006-57-3 1L-3,4:5,6-Di-O-isopropyliden-1,2-di-O-tosyl-chiro-inosit 
• 6770-74-7 1L-2,3,4,5,6-Penta-O-benzoyl-1-O--chiro-inosit 
• 80177-95-3 1L-2,3:5,6-Di-O-isopropyliden-1-O-tosyl-chiro-inosit 
• 18391-53-2 1L-3,4:5,6-Di-O-isopropyliden-1-O-tosyl-chiro-inosit 

Relevant academic research and scientific papers

Synthesis and evaluation of 3-modified 1D-myo-inositols as inhibitors and substrates of phosphatidylinositol synthase and inhibitors of myo-inositol uptake by cells

A number of 3-substituted 1D-myo-inositols were synthesized and evaluated as substrates for phosphatidylinositol synthase and uptake by intact cells. 1D-3-Amino-, -3-chloro-, and -3-(acetylthio)-3-deoxy-myo-inositols were all synthesized by nucleophilic d

Cyclitol Reactions, IV. Synthesis of Enantiomeric Conduritols and Amino-Conduritols

The key-intermediate for all syntheses described in this paper is the 1-O-tosylate 7 of quebrachitol (1).This leads, via 8, to the 1L-conduritol B (5) and, via 13, to the 1L-conduritol F (17).Selective displacement of the equatorial tosyloxy group in comp