2‘-Deoxy-3-isoadenosine Forms Hoogsteen-Type Base Pairs with Thymidine in the d(CG[iA]TCG)2 Duplex1
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 118 (12) , 3065-3066
- https://doi.org/10.1021/ja954178a
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- DNA Triplexes: Solution Structures, Hydration Sites, Energetics, Interactions, and FunctionBiochemistry, 1994
- Water Ring Structure at DNA Interfaces: Hydration and Dynamics of DNA-Anthracycline ComplexesBiochemistry, 1994
- Structural analysis of drug—DNA interactionsCurrent Opinion in Structural Biology, 1991
- The allylic protection method in solid-phase oligonucleotide synthesis. An efficient preparation of solid-anchored DNA oligomersJournal of the American Chemical Society, 1990
- DNA-drug interactionsJournal of Molecular Biology, 1989
- Synthesis of 3-(2'-deoxy-D-erythro-pentofuranosyl)adenine. Application of a new protecting group, pivaloyloxymethyl(Pom)Journal of the American Chemical Society, 1967
- Synthesis and Properties of Analogs of Adenosine Diphosphate, Adenosine Triphosphate, and Nicotinamide-Adenine Dinucleotide Derived from 3-β-D-Ribofuranosyladenine (3-Isoadenosine)*Biochemistry, 1965