Synthesis of α-trinositol analogues derived from D-(-)-quinic acid as affinity probe precursors
Guédat, P. ; Rehnberg, N. LU
; Spiess, B.
and Schlewer, G.
(1997)
In Synlett
1997(5).
p.553-554
- Abstract
D-(-)-Quinic acid was appropriately protected to permit the phosphorylation of the three vicinal hydroxyl groups. Final deprotection lead to tris(phosphates) possessing the same configuration as the parent α-trinositol and an arm suitable for the attachement of a photoactivable group.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/3178de70-38eb-41fe-82d3-f053e15ef2d2
- author
- Guédat, P.
; Rehnberg, N.
LU
; Spiess, B.
and Schlewer, G.
- publishing date
- 1997-05
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Synlett
- volume
- 1997
- issue
- 5
- pages
- 2 pages
- publisher
- Georg Thieme Verlag
- external identifiers
-
- scopus:0343466800
- ISSN
- 0936-5214
- DOI
- 10.1055/s-1997-3205
- language
- English
- LU publication?
- no
- id
- 3178de70-38eb-41fe-82d3-f053e15ef2d2
- date added to LUP
- 2021-11-11 13:03:34
- date last changed
- 2022-02-02 01:16:14
@article{3178de70-38eb-41fe-82d3-f053e15ef2d2,
abstract = {{<p>D-(-)-Quinic acid was appropriately protected to permit the phosphorylation of the three vicinal hydroxyl groups. Final deprotection lead to tris(phosphates) possessing the same configuration as the parent α-trinositol and an arm suitable for the attachement of a photoactivable group.</p>}},
author = {{Guédat, P. and Rehnberg, N. and Spiess, B. and Schlewer, G.}},
issn = {{0936-5214}},
language = {{eng}},
number = {{5}},
pages = {{553--554}},
publisher = {{Georg Thieme Verlag}},
series = {{Synlett}},
title = {{Synthesis of α-trinositol analogues derived from D-(-)-quinic acid as affinity probe precursors}},
url = {{http://dx.doi.org/10.1055/s-1997-3205}},
doi = {{10.1055/s-1997-3205}},
volume = {{1997}},
year = {{1997}},
}