117666-30-5Relevant academic research and scientific papers
The preparation and phosphorylation of 2,5- and 1D-2,6-di-O-benzyl-myo-inositol
Desai,Gigg,Gigg,Payne
, p. 65 - 79 (2007/10/02)
1,3,4,6-Tetra-O-allyl-myo-inositol was converted into the 2,5-di-O-benzyl- and 2,5-di-O-p-methoxybenzyl ethers, and the products were deallylated to give the 2,5-di-O-benzyl (and p-methoxybenzyl) ethers of myo-inositol, which were converted into the mono-
An efficient chemoenzymic access to optically active myo-inositol polyphosphates
Gou,Liu,Chen
, p. 51 - 64 (2007/10/02)
The 1,4,5-tris-, 1,3,4-tris-, and 1,3,4,5-tetrakis-phosphates of 1D-myo-inositol have been prepared in their enantiomerically pure forms from the two enantiomers of 1,2:5,6-di-O-cyclohexylidene-myo-inositol. A facile enzymic preparation is also described
AN EFFICIENT ROUTE TO D-MYO-INOSITOL 1,3,4-TRIPHOSPHATE AND D-MYO-INOSITOL 1,3,4,5-TETRAKISPHOSPHATE
Gou, Da-Ming,Chen, Ching-Shih
, p. 721 - 724 (2007/10/02)
Multigram quantities of the title compounds in their enantiomerically-pure forms have been prepared by employing a chiral precursor which can be obtained via a facile enzymatic process.
TOTAL SYNTHESIS OF OPTICALLY ACTIVE MYO-INOSITOL 1,4,5-TRISPHOSPHATE AND MYO-INOSITOL 1,3,4,5-TETRAKISPHOSPHATE
Dreef, C. E.,Tuinman, R. J.,Elie, C. J. J.,Marel, G. A. van der,Boom, J. H. van
, p. 395 - 397 (2007/10/02)
A convenient approach to the preparation of the title compounds illustrating selective protection, optical resolution and phosphorylation is presented.
