New nucleoside analogues for the recognition of pyrimidine-purine inversion sites
| Data(s) |
2003
|
|---|---|
| Resumo |
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 |
| Formato |
application/pdf |
| Identificador |
http://boris.unibe.ch/68568/1/10833739.pdf 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 <http://dx.doi.org/10.1081/NCN-120022835> doi:10.7892/boris.68568 info:doi:10.1081/NCN-120022835 info:pmid:14565379 urn:issn:1525-7770 |
| Idioma(s) |
eng |
| Publicador |
Taylor & Francis |
| Relação |
http://boris.unibe.ch/68568/ |
| Direitos |
info:eu-repo/semantics/restrictedAccess |
| Fonte |
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 <http://dx.doi.org/10.1081/NCN-120022835> |
| Palavras-Chave | #570 Life sciences; biology #540 Chemistry |
| Tipo |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion PeerReviewed |
