## Abstract Immobilized and fully protected oligodeoxynucleotides containing a 4‐(1,2,4‐triazolyl)‐thymidine residue at a predetermined position were prepared according to a well‐established phosphite triester methodology using 2‐cyanoethyl phosphoramidites of a 4‐(1,2,4‐triazolyl)‐substituted thym
Solid-phase synthesis of oligodeoxynucleotides containing 6-O-alkylguanosines
✍ Scribed by H. C. P. F. Roelen; H. F. Brugghe; H. van den Elst; J. C. Klein; G. A. van der Marel; J. H. van Boom
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 929 KB
- Volume
- 111
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
High‐quality oligodeoxynucleotides having an 6‐O‐alkyl‐2′‐deoxyguanosine (alkyl = methyl, ethyl, n‐propyl or n‐hexyl) residue at a predetermined position can be obtained via a solid‐phase approach using the respective 2‐cyanoethyl N,N‐diisopropylphosphoramidites of 5′‐O‐(4.4′‐dimethoxytrityl)‐protected 6‐O‐alkyl‐2′‐deoxyguanosines having a free exocyclic amino group, and 5′‐O‐(4‐4′‐dimethoxytrityl) N‐acyl‐protected (i.e., benzoyl and isobutyryl for dC/dA and dG, respectively) 2′‐deoxynucleosides.
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