Synthesis of oligodeoxynucleotides containing thymidines linked via an internucleosidic-(3′-5′)-methylene bond
✍ Scribed by G. H. Veeneman; G. A. van der Marel; H. van den Elst; J. H. van Boom
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 263 KB
- Volume
- 109
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
Condensation of N^3^‐benzoyl‐5′‐O‐dimethoxytrityl‐3′‐O‐(4‐penten‐1‐oxymethyl)‐thymidine with N^3^‐benzoyl‐3′‐O‐methoxyacctyl‐thymidine, in the presence of N‐iodosuccinimide, afforded a fully‐protected thymidine dimer having an internucleosidic‐(3′‐5′)‐methylene linkage. The latter was utilized in the preparation, in solution and on a solid support, of DNA‐fragments containing one or more T‐CH~2~‐T dimer(s).
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Linked symmetrical [3] and [5]rotaxanes consisting of an oligomeric phenylene ethynylene (OPE) framework as a p-conjugated guest moiety and lipophilic permethylated a-cyclodextrins (PM a-CDs), as macrocyclic hosts have been prepared by double intramolecular self-inclusion of an OPE guest unit carryi