A search for quantitative acylation of α-trinositol (1D-myo-inositol 1,2,6-tris(dihydrogen phosphate) pentasodium salt)

Article abstract of DOI:10.1080/07328309608005666

The acylation of α-trinositol is very sensitive to reaction conditions. Competing condensation reactions may give pyrophosphates and cyclic phosphates. Treatment of a tert-ammonium salt corresponding to α-trinositol with carboxylic acid anhydride and DMAP gives a good yield of the expected esters.

Full text of DOI:10.1080/07328309608005666

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Journal of Carbohydrate Chemistry
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A Search for Quantitative Acylation
of α-Trinositol (1d-myo-Inositol 1,2,6-
tris(dihydrogen phosphate) Pentasodium
Salt)
Mats Malmberg a & Nicola Rehnberg b
a Synthelec AB , Ideon, S-223 70, Lund, Sweden
b Perstorp Pharma , S-284 80, Perstorp, Sweden
Published online: 22 Aug 2006.
To cite this article: Mats Malmberg & Nicola Rehnberg (1996) A Search for Quantitative Acylation
of α-Trinositol (1d-myo-Inositol 1,2,6-tris(dihydrogen phosphate) Pentasodium Salt), Journal of
Carbohydrate Chemistry, 15:4, 459-464, DOI: 10.1080/07328309608005666
To link to this article: http://dx.doi.org/10.1080/07328309608005666
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