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Attachment to Nucleobases

Base modification at the 4-position of pyrimidines leads to loss of base-pairing properties. The thiol moiety in 91 was deprotected after ODN synthesis using 1 M DBU in acetonitrile. The modified oligothymidylate was then cleaved from the solid phase and reacted with N-(2-chloroethylthio)phthalimide to yield 92, which was subjected to further derivatization [264]. Purine base positions accessible for ligand attachment are C-8 of adenosine (93) [265] and C-2 of guanosine (94) [266]. [Pg.306]


Transition metal ion incorporation in hybrid inorganic-nucleic acid structures adds another dimension to the field of DNA nanotechnology because metal ions, in particular those with unpaired d electrons, have a broad range of electronic and magnetic properties. In most applications in material science, DNA is used as a scaffold for uniform binding of metal ions either to nucleobases or to ligands attached to nucleobases. For example, Braun et al. [Pg.547]

DNA labelled through attachment to nucleobases has been prepared using 4-A(- 6-(y-... [Pg.275]


See other pages where Attachment to Nucleobases is mentioned: [Pg.661]    [Pg.306]   


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