Literature DB >> 12007477

Synthesis of a globotetraose trimer.

Anders Bergh1, Sumita Bhattacharyya, Ulf J Nilsson.   

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.

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Year:  2002        PMID: 12007477     DOI: 10.1016/s0008-6215(02)00080-0

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  2 in total

Review 1.  Sphingolipidomics: methods for the comprehensive analysis of sphingolipids.

Authors:  Christopher A Haynes; Jeremy C Allegood; Hyejung Park; M Cameron Sullards
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2008-12-31       Impact factor: 3.205

2.  Conjugation of carbohydrates to proteins using di(triethylene glycol monomethyl ether) squaric acid ester revisited.

Authors:  Peng Xu; Michael N Trinh; Pavol Kováč
Journal:  Carbohydr Res       Date:  2017-11-07       Impact factor: 2.104

  2 in total

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