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
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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