68134-83-8Relevant articles and documents
Analysis of the Chirality of 16O, 17O, 18O> Phosphate Esters by 31P Nuclear Magnetic Resonance Spectroscopy
Jarvest, Richard L.,Lowe, Gordon,Potter, Barry V. L.
, p. 3186 - 3195 (2007/10/02)
A stereospecific method for cyclising D-glucose 6-16O, 17O, 18O>phosphate and adenosine 5'-16O, 17O, 18O>-phosphate to their conformationally locked six-membered cyclic phosphate diesters has been developed.Using 16O, 17O, 18O>phosphate esters of known absolute configuration it is shown by 31P n.m.r. spectroscopy, after esterification to the axial and equatorial triesters, that the cyclisation occurs with inversion of configuration.It is now possible, therefore, to determine the chirality at phosphorus of D-glucose 6-16O, 17O, 18O>phosphate and adenosine 5'-16O, 17O, 18O>phosphate by this procedure.