Items where Author is "Blindauer, C. A."

2015

Blindauer, C. A. and Sigel, A. and Operschall, B. P. and Griesser, R. and Holy, A. and Sigel, H.. (2015) Extent of Intramolecular π-Stacks in Aqueous Solution in Mixed-Ligand Copper(II) Complexes Formed by Heteroaromatic Amines and the Anticancer and Antivirally Active 9-[2-(Phosphonomethoxy)ethyl]guanine (PMEG). A Comparison with Related Acyclic Nucleotide Analogues. Polyhedron, 103, Part B. pp. 248-260.

2013

Blindauer, C. A. and Sigel, A. and Operschall, B. P. and Holy, A. and Sigel, H.. (2013) Extent of Intramolecular π-Stacks in Aqueous Solution in Mixed-Ligand CopperII) Complexes Formed by Heteroaromatic Amines and 1-[2-(Phosphonomethoxy)ethyl]cytosine (PMEC), a Relative of Antivirally Active Acyclic Nucleotide Analogues. Zeitschrift für anorganische und allgemeine Chemie, Bd. 639, H. 8-9. pp. 1661-1673.

2012

Gómez-Coca, R. B. and Blindauer, C. A. and Sigel, A. and Operschall, B. P. and Holy´, A. and Sigel, H.. (2012) Extent of Intramolecular Pi-Stacks in Aqueous Solution in Mixed-Ligand Copper(II) Complexs Formed by Heteroaromatic Amines and Several 2-Aminopurine Derivatives of the Antivirally Active Nucleotide Analogue 9-[2-(Phosphonomethoxy)ethyl]adenine (PMEA). (Ternary Complexes in Solution. Part 71). Chemistry & biodiversity, Vol. 9, H. 9. pp. 2008-2034.

1999

Sigel, H. and Song, B. and Blindauer, C. A. and Kapinos, L. E. and Gregávn, F. and Prónayová, N.. (1999) Why is the antiviral nucleotide analogue 9-[2-(phosphonomethoxy)ethyl]adenine in its diphosphorylated form (PMEApp4–) initially a better substrate for polymerases than (2′-deoxy)adenosine 5′-triphosphate (dATP4–/ATP4–)? Considerations on the mechanism of nucleic acid polymerases. Chemical Communications, 35 (8). pp. 743-744.