123270-13-3

Upstream product

• 87-89-8 D-myo-inositol 
• 69304-37-6 1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane 

Downstream Products

• 193688-97-0 Phosphoric acid benzyl ester methyl ester (1R,2S,3R,4R,5S,6R)-2,3,4,5,6-pentahydroxy-cyclohexyl ester 
• 193688-99-2 Phosphoric acid benzyl ester (1S,2S,3S,4R,5R,6R)-4-(bis-benzyloxy-phosphoryloxy)-2,3,5,6-tetrahydroxy-cyclohexyl ester methyl ester 
• 193688-93-6 Phosphoric acid benzyl ester (5aS,6R,6aR,11aS,12R,12aR)-12-hydroxy-2,2,4,4,8,8,10,10-octaisopropyl-hexahydro-1,3,5,7,9,11-hexaoxa-2,4,8,10-tetrasila-benzo[1,2;4,5]dicyclohepten-6-yl ester methyl ester 
• 193688-95-8 Phosphoric acid benzyl ester (5aR,6S,6aS,11aS,12R,12aR)-12-(bis-benzyloxy-phosphoryloxy)-2,2,4,4,8,8,10,10-octaisopropyl-hexahydro-1,3,5,7,9,11-hexaoxa-2,4,8,10-tetrasila-benzo[1,2;4,5]dicyclohepten-6-yl ester methyl ester 
• 123355-55-5 2-O,5-O-dibenzoyl-myo-inositol 
• 138343-44-9 myo-inositol 2,5-dinitrate 

Relevant academic research and scientific papers

Regioselective functionalization of unprotected myo-inositol by electrophilic substitution

Unprotected myo-inositol was treated with various electrophiles, such as aroyl chlorides, tosyl chloride and tert-butyldiphenylsilyl chloride in a solution of LiCl/DMA or DMSO to afford regioselectively 1,3-di-O-substituted or racemic 1-O-substituted deri

One-step regioselective functionalization of myo-inositol by dissolution strategy

Functionalizations of hydroxy groups of myo-inositol were usually nonselective due to its poor solubility. By dissolving myo-inositol in DMSO or LiCl-N,N-dimethylacetamide, we have achieved regioselective acylation, silylation, sulfonylation, phosphinylat

Highly Efficient Protection by the Tetraisopropyldisiloxane-1,3-diyl Group in the Synthesis of myo-Inositol Phosphates as Inositol 1,3,4,6-tetrakisphosphate

Regioselective introduction of the tetraisopropyldisiloxane-1,3-diyl group onto myo-inositol and 1,2-O-cyclohexylidene-myo-inositol realised the efficient synthesis of various myo-inositol phosphates.