Block synthesis of oligonucleotides by the phosphotriester approach
β Scribed by N.J. Cusack; C.B. Reese; J.H. van Boom
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- French
- Weight
- 261 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Most of the published work on the chemical synthesis of oligonucleotides* has involved the us8 of intermediates with unprotected lnternucleotide phosphodiester linkages. Such intermediates can usually be isolated only on a comparatively small scale and are sometimes difficult to obtain pure. Furthermore, the presence of free phosphodieeter functions can lead to undesirable eidereactions during subeequent phosphorylation steps. This presumably accounts for the low yields, especially of larger oligomers, often obtained by this approach.
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4,6-Dinitro-l-(mesitylene-2-sulphonyloxy)-benzotriazole [DMBT, (@)I, l-(mesitylene-2-sulphonyloxy)-4-nitro-6-trifluoromethylbenzotriazole (@) and 1-(mesitylene-2-sulphonyl)-4nitro-1,2,3-triazole [iso-MSNT, (211 are more reactive condensing agents in the phosphotriester approach to oligonucleotide sy
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