128459-28-9

Upstream product

• 87-89-8 D-myo-inositol 
• 109280-15-1 (1R)-(+)-camphor dimethyl acetal 
• 100-39-0 benzyl bromide 
• 142534-51-8 C₄₂H₆₀O₉Si₂ 
• 128459-27-8 1D-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol 

Downstream Products

• 24558-77-8 3,4,5,6-tetra-O-benzyl inositol 
• 28140-40-1 1,4,5,6-tetra-O-benzyl-myo-inositol 
• 128459-27-8 1D-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol 

Relevant academic research and scientific papers

Efficient and systematic syntheses of enantiomerically pure and regiospecifically protected myo-inositols

Efficient and systematic syntheses of a variety of enantiomerically pure and regiospecifically protected myo-inositols, which can be readily used as precursors for most natural and unnatural derivatives of myo-inositol, have been developed. The key strate

The synthesis of homochiral inositol phosphates from myo-inositol

A new synthetic procedure for efficient conversion of myo-inositol into homochiral inositol phosphates is presented, and is illustrated with total synthesis of myo-inositol 1-phosphate, 2-deoxy-myo-inositol 1-phosphate, myo-inositol 3-phosphate, myo-inosi

Synthesis of the enantiomeric 1,4,5,6-tetra-O-benzyl-myo inositols

The synthesis of the optically pure 1,4,5,6-tetra-O-benzyl-myo-inositols was achieved in four steps via diastereomeric 2,3-spiro-acetals of myo-inositol with l- and d-camphor as the key intermediates. Camphor dimethyl acetal was used for the acetalation r