18779-66-3

Upstream product

• 87-89-8 D-myo-inositol 
• 98-59-9 p-toluenesulfonyl chloride 
• 4307-26-0 2,4,5,6-Tetra-O-acetyl-1,3-bis-O-p-toluolsulfonyl-myo-inosit 

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