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The use of liquid phase carriers for large scale oligonucleotide synthesis in solution via phosphoamidite chemistry

✍ Scribed by Ralf Wörl; Hubert Köster


Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
821 KB
Volume
55
Category
Article
ISSN
0040-4020

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✦ Synopsis


Nucleoside derivatives coupled to a multifunctional highly symmetric primary amine 3 built the fundamental of a convenient method for large scale oligonucleotide synthesis in solution. The basic purification for the fast isolation of intermediates is obtained by gel permeation chromatography. Monomer and dimer phosphoamidites (la-d; 2a, b) are used for the preparation of short oligodeoxynucleotides. Total cycle yields between 81 and 95 % and average cycle yields of 87 % were obtained. MALDI-TOF-mass spectrometry was used for the analysis of the fully protected intermediates during synthesis.


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Synthesis of new liquid phase carriers f
✍ Ralf Wörl; Hubert Köster 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 878 KB

The synthesis of multifunctional symmetric primary amines 4 and 8 and the covalent binding of 5'-0dimethoxytrityl-deoxynucleoside derivatives to their amino groups (compound 5 and 9) is described. Different strategies for dedimethoxytritylation including the use of strong acidic ion exchangers or pr