Synthesis and Stability of Oligonucleotides Containing Acyclic Achiral Nucleoside Analogues with Two Base Moieties
Author:
Affiliation:
1. Laboratory of Medicinal Chemistry, Rega Institute for Medicinal Research, Katholieke Universiteit Leuven, Minderbroedersstraat 10, B-3000 Leuven, Belgium
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol0360647
Reference13 articles.
1. Molecular Structure of Nucleic Acids: A Structure for Deoxyribose Nucleic Acid
2. Functionalization of Oligonucleotides with Amino Groups and Attachment of Amino Specific Reporter Groups
3. Functionalization of Oligonucleotides by the Incorporation of Thio-Specific Reporter Groups
4. Efficient guanidination of the phosphate linkage towards cationic phosphoramidate oligonucleotides
5. Synthesis, enzymatic stability and base-pairing properties of oligothymidylates containing thymidine dimers with different N-substituted guanidine linkages
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