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Synthesis of a globotetraose trimer.

Bergh, Anders; Bhattacharyya, Sumita and Nilsson, Ulf LU (2002) In Carbohydrate Research 337(10). p.947-949
Abstract
The synthesis is described of a globotetraose trimer in 74% yield by the reaction of tris(2-aminoethyl)amine with the hydrophobic squaric decyl ester glycoside of globotetraose. The synthesis was readily monitored and purified using reversed phase HPLC. Unreacted squaric decyl ester globotetraoside was recovered rendering the method highly economical.
Please use this url to cite or link to this publication:
author
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Carbohydrate Research
volume
337
issue
10
pages
947 - 949
publisher
Elsevier
external identifiers
  • pmid:12007477
  • wos:000175917500008
  • scopus:0037071148
ISSN
1873-426X
DOI
10.1016/S0008-6215(02)00080-0
language
English
LU publication?
yes
id
70735b93-93fd-484a-b7e8-87cbeadf1245 (old id 108185)
date added to LUP
2007-07-10 09:08:12
date last changed
2017-01-01 04:19:50
@article{70735b93-93fd-484a-b7e8-87cbeadf1245,
  abstract     = {The synthesis is described of a globotetraose trimer in 74% yield by the reaction of tris(2-aminoethyl)amine with the hydrophobic squaric decyl ester glycoside of globotetraose. The synthesis was readily monitored and purified using reversed phase HPLC. Unreacted squaric decyl ester globotetraoside was recovered rendering the method highly economical.},
  author       = {Bergh, Anders and Bhattacharyya, Sumita and Nilsson, Ulf},
  issn         = {1873-426X},
  language     = {eng},
  number       = {10},
  pages        = {947--949},
  publisher    = {Elsevier},
  series       = {Carbohydrate Research},
  title        = {Synthesis of a globotetraose trimer.},
  url          = {http://dx.doi.org/10.1016/S0008-6215(02)00080-0},
  volume       = {337},
  year         = {2002},
}