
TY  - JOUR
A1  - Angyal, SJ 
A1  - Russell, AF 
T1  - Cyclitols. XXIX. Polyphosphorylation of polyols. The synthesis of myo-inositol pentaphosphates
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1969
VL  - 22
IS  - 2
SP  - 391
EP  - 404
KW  - 
UR  - https://doi.org/10.1071/CH9690391 
N2  - Heating myo-inositol with an excess of the triethylammonium salt of N- benzoylphosphoramidic acid in N,N-dimethylformamide results in phosphorylation of every hydroxyl group. The method appears to be general for the complete phosphorylation of unsubstituted or partially substituted inositols. Starting with 1-O-benzyl- and 4-O-benzyl-myo- inositol, phosphorylation and subsequent hydrogenolysis gave DL-myo- inositol 1,2,4,5,6- and 1,2,3,4,5-pentaphosphate, respectively. Other methods of phosphorylation were found unsuitable. 
ER  -

