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. Furthe
Highly reactive condensing agents for the synthesis of oligonucleotides by the phosphotriester approach
β Scribed by Kevin G. Devine; Colin B. Reese
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 300 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
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 synthesis than 1-(mesitylene-2-sulphonylj-3-nitro-1,2,4triaaole [MSNT, (&)I by factors of at least 10, ~a. 4 and ~a. 1.3, respectively.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
It was shown that arylsulfonyl chlorides in the presence of N-methylimidazole are powerful condensing agents for the triester internucleotide bond formation.