A search for quantitative acylation of α-trinositol (1D-myo-inositol 1,2,6-tris(dihydrogen phosphate) pentasodium salt)
Malmberg, Mats and Rehnberg, Nicola LU
(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.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/be67029e-2670-4e01-8a6b-32634ada809e
- 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
- Taylor & Francis
- 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
- 2025-10-14 11:07:07
@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 = {{Taylor & Francis}},
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}},
}