Buchini, S.; Leumann, Christian (2003). New nucleoside analogues for the recognition of pyrimidine-purine inversion sites. Nucleosides, nucleotides & nucleic acids, 22(5-8), pp. 1199-1201. Taylor & Francis 10.1081/NCN-120022835
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A new nucleoside designed to enhance triplex stability has been synthesised in 15 steps starting from sugar 2. This pathway contains the sugar derivative 9 which is a useful intermediate for the introduction of other natural and unnatural bases into the 2'-aminoethoxy nucleoside containing scaffold
Item Type: |
Journal Article (Original Article) |
|---|---|
Division/Institute: |
08 Faculty of Science > Department of Chemistry, Biochemistry and Pharmaceutical Sciences (DCBP) |
UniBE Contributor: |
Leumann, Christian |
Subjects: |
500 Science > 570 Life sciences; biology 500 Science > 540 Chemistry |
ISSN: |
1525-7770 |
Publisher: |
Taylor & Francis |
Language: |
English |
Submitter: |
Christian Leumann |
Date Deposited: |
19 May 2015 08:52 |
Last Modified: |
05 Dec 2022 14:46 |
Publisher DOI: |
10.1081/NCN-120022835 |
PubMed ID: |
14565379 |
Additional Information: |
Notes: Department of Chemistry and Biochemistry, University of Bern, Bern, Switzerland buchini@iocunibechFAU - Buchini, Sabrina |
Uncontrolled Keywords: |
analogue analogues base bases Binding Sites chemical synthesis chemistry DNA inversion Nucleic Acid Conformation nucleoside nucleoside analogues nucleosides Purines Pyrimidines recognition site stability sugar Triplex |
BORIS DOI: |
10.7892/boris.68568 |
URI: |
https://boris.unibe.ch/id/eprint/68568 |
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