138480-22-5

Upstream product

• 128459-27-8 1D-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol 
• 109280-15-1 (1R)-(+)-camphor dimethyl acetal 
• 138480-20-3 D-1,4,5-tri-O-trimethylacetyl-2,3-O-(D-1,7,7-trimethyl<2.2.1>bicyclohept-2-ylidene)-myo-inositol 
• 100-39-0 benzyl bromide 
• 138480-21-4 D-6-O-benzyl-2,3-O-(D-1,7,7-trimethyl<2.2.1>bicyclohept-2-ylidene)-1,4,5-tri-O-trimethyl-acetyl-myo-inositol 

Downstream Products

• 138480-23-6 D-6-O-benzyl-2,3-O-(D-1,7,7-trimethyl<2.2.1>bicyclohept-2-ylidene)-1,4,5-tri-O-(2-oxo-5,6-benzo-1,3,2-dioxaphosphep-2-yl)myo-inositol 
• 2068-89-5 D-myo-inositol 1,4,5-triphosphate 

Relevant academic research and scientific papers

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

Expedient Synthesis of D-myo-Inositol 1,4,5-Trisphosphate and D-myo-Inositol 1,4-Bisphosphate

Readily available selfresolving myo-inositol D-camphor 2,3-monoacetal is converted into the title inositol phosphates by the concise procedures utilizing 1,4,5-selective tris-acylation and 1,4-selective bis-silylation of the starting tetrol in the key ste