120401-18-5

Upstream product

• 39637-74-6 (1S)-(-)-camphanic chloride 
• 85747-85-9 (1S,2S,3R,4S,5R,6R)-2,3,4,5-Tetrakis-benzyloxy-6-fluoro-cyclohexanol 
• 26276-99-3 rac-1,4,5,6-tetra-O-benzyl-myo-inositol 
• 23262-92-2 (+/-)-1-O-benzoyl-3,4,5,6-tetra-O-benzyl-myo-inositol 
• 85716-58-1 DL-2-O-Benzoyl-3,4,5,6-tetra-O-benzyl-1-deoxy-1-fluoro-scyllo-inositol 

Downstream Products

• 120444-21-5 (1R,2R,3S,4R,5S,6S)-2,3,4,5-Tetrakis-benzyloxy-6-fluoro-cyclohexanol 
• 120444-23-7 (+)-1L-3,4,5,6-Tetra-O-benzyl-1-deoxy-1-fluoro-myo-inositol 
• 214154-08-2 D-1,4,5,6-tetra-O-benzyl-2,3-dideoxy-2,3-difluoro-myo-inositol 

Relevant academic research and scientific papers

Synthesis of D-1,2-dideoxy-1,2-difluoro-myo-inositol 3,4,5,6-tetrakisphosphate and its enantiomer as analogues of myo-inositol 3,4,5,6-tetrakisphosphate

DL-3,4,5,6-Tetra-O-benzyl-1-deoxy-1-fluoro-scyllo-inositol was resolved using (-)-(1S, 4R)-camphanyl chloride. The diastereoisomers formed were separated and the structure of D-3,4,5,6-tetra-O-benzyl-2-(1S,4R)-camphanyl-1-deoxy-1-fluoro-scyllo-inositol wa

A Synthesis of (-)-1L-1-Deoxy-1-fluoro-myo-inositol; a Compound of Potential Use in sorting out the Phosphatidylinositol Response

A synthesis of 1L-1-deoxy-1-fluoro-myo-inositol in optically pure form starting from myo-inositol is reported.