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

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

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Item Type:

Journal Article (Original Article)

Division/Institute:

08 Faculty of Science > Departement of Chemistry and Biochemistry

UniBE Contributor:

Leumann, Christian

Subjects:

500 Science > 570 Life sciences; biology
500 Science > 540 Chemistry

ISSN:

0002-7863

Publisher:

American Chemical Society

Language:

English

Submitter:

Christian Leumann

Date Deposited:

20 May 2015 14:05

Last Modified:

20 May 2015 14:05

Publisher DOI:

10.1021/ja9704904

Uncontrolled Keywords:

2-Aminopyridine C-nucleosides cytidine replacement DNA helix HELIX FORMATION py-pu-py Selectivity specificity triple triple helix

BORIS DOI:

10.7892/boris.68617

URI:

https://boris.unibe.ch/id/eprint/68617

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