5-Substituted 2-Aminopyridine C-nucleosides as protonated cytidine equivalents: Increasing efficiency and selectivity in DNA triple helix formation
Data(s) |
1997
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Formato |
application/pdf |
Identificador |
http://boris.unibe.ch/68617/1/ja9704904.pdf Hildbrand, S.; Blaser, A.; Parel, S. P.; Leumann, Christian (1997). 5-Substituted 2-Aminopyridine C-nucleosides as protonated cytidine equivalents: Increasing efficiency and selectivity in DNA triple helix formation. Journal of the American Chemical Society, 119(24), pp. 5499-5511. American Chemical Society 10.1021/ja9704904 <http://dx.doi.org/10.1021/ja9704904> doi:10.7892/boris.68617 info:doi:10.1021/ja9704904 urn:issn:0002-7863 |
Idioma(s) |
eng |
Publicador |
American Chemical Society |
Relação |
http://boris.unibe.ch/68617/ |
Direitos |
info:eu-repo/semantics/restrictedAccess |
Fonte |
Hildbrand, S.; Blaser, A.; Parel, S. P.; Leumann, Christian (1997). 5-Substituted 2-Aminopyridine C-nucleosides as protonated cytidine equivalents: Increasing efficiency and selectivity in DNA triple helix formation. Journal of the American Chemical Society, 119(24), pp. 5499-5511. American Chemical Society 10.1021/ja9704904 <http://dx.doi.org/10.1021/ja9704904> |
Palavras-Chave | #570 Life sciences; biology #540 Chemistry |
Tipo |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion PeerReviewed |