Synthesis, enzymatic stability and physicochemical properties of oligonucleotides containing a N-cyanoguanidine linkage.
โ Scribed by C. Pannecouque; F. Vandendriessche; J. Rozenski; G. Janssen; R. Busson; A. Van Aerschot; P. Claes; P. Herdewijn
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 900 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
โฆ Synopsis
Nuclewide dimers witb a Nsyanoguanidine linkage were syntbesked and used as building blocks for oligonwkotide synthesis. Oligonwkotides composed of alternating phosphod.iester and cyanoguaoidine functions are still able to hybridize with a complementary natural oligodeoxynucleotide.
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The synthesis of 5,6-bicyclic thymine:thymine nucleoside containing a conformationally restricted dioxane acetal has been achieved from 2'-O-allyl 5-methyl uridine. The two diastereomers were separated and incorporated in a single position within an oligonucleotide (ON) sequence. The binding propert