Chiral synthesis of D- and L-myo-inositol 1,4,5-trisphosphate

Chiral inositols (D-chiro-inositol from D-pinitol and L-chiro-inositol from L-quebrachitol) were converted to the 3,4-di-O-benzyl ethers, which were selectively benzoylated to yield the 1,2,5-tri-O-benzoyl-3,4-di-O-benzyl-chiro-inositols. The free hydroxyl group in each derivative was inverted by wa...

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Veröffentlicht in:	Proceedings of the National Academy of Sciences - PNAS 1989-01, Vol.86 (1), p.94-98
Hauptverfasser:	Tegge, W, Ballou, C E
Format:	Artikel
Sprache:	eng
Schlagworte:	Chromatography, High Pressure Liquid Indicators and Reagents Inositol 1,4,5-Trisphosphate Inositol Phosphates - chemical synthesis Magnetic Resonance Spectroscopy Molecular Structure Optical Rotation Stereoisomerism Sugar Phosphates - chemical synthesis
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