Abstract
We describe the synthesis of a hybrid DNA/organic macrocycle that is prepared by formation of an amide linkage across one full turn of DNA. Formation of a catenane proved that the linkage crossed a turn rather than running along the phosphodiester backbone contour. the product, a doubly tailed catenane, contains 5'- and 3'-termini that can be functionalized further or used to incorporate the catenane structure into other DNA assemblies.
| Original language | American English |
|---|---|
| Journal | Journal of the American Chemical Society |
| Volume | 130 |
| DOIs | |
| State | Published - Aug 1 2008 |
Keywords
- Anthracenes
- Catenane
- DNA
- DNA Cleavage
- DNA Helix
- DNA Hybrid
- DNA Strand
- DNA Structure
- DNA Template
- Denaturation
- Molecular Structure
- Nucleic Acid Conformation
- Oligonucleotide
- Oligonucleotides
- Stereoisomerism
- Synthesis
- Ultraviolet Rays
Disciplines
- Chemistry
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