A search for quantitative acylation of α-trinositol (1D-myo-inositol 1,2,6-tris(dihydrogen phosphate) pentasodium salt)
(1996) In Journal of Carbohydrate Chemistry 15(4). p.459-464- Abstract
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.
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- author
- Malmberg, Mats and Rehnberg, Nicola LU
- publishing date
- 1996
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Journal of Carbohydrate Chemistry
- volume
- 15
- issue
- 4
- pages
- 6 pages
- publisher
- Marcel Dekker
- external identifiers
-
- scopus:0007763501
- ISSN
- 0732-8303
- DOI
- 10.1080/07328309608005666
- language
- English
- LU publication?
- no
- id
- be67029e-2670-4e01-8a6b-32634ada809e
- date added to LUP
- 2021-11-11 12:38:25
- date last changed
- 2022-02-02 01:16:14
@article{be67029e-2670-4e01-8a6b-32634ada809e, abstract = {{<p>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.</p>}}, author = {{Malmberg, Mats and Rehnberg, Nicola}}, issn = {{0732-8303}}, language = {{eng}}, number = {{4}}, pages = {{459--464}}, publisher = {{Marcel Dekker}}, series = {{Journal of Carbohydrate Chemistry}}, title = {{A search for quantitative acylation of α-trinositol (1D-myo-inositol 1,2,6-tris(dihydrogen phosphate) pentasodium salt)}}, url = {{http://dx.doi.org/10.1080/07328309608005666}}, doi = {{10.1080/07328309608005666}}, volume = {{15}}, year = {{1996}}, }