5-Substituted 2-Aminopyridine C-nucleosides as protonated cytidine equivalents: Increasing efficiency and selectivity in DNA triple helix formation


Autoria(s): Hildbrand, S.; Blaser, A.; Parel, S. P.; Leumann, Christian
Data(s)

1997

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