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

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Number of items: 4.

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.

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