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- URN to cite this document:
- urn:nbn:de:bvb:355-epub-200430
- DOI to cite this document:
- 10.5283/epub.20043
Alternative links to fulltext:DOI
Abstract
The azides 1 and 2 bearing a phenoxazinium and a coumarin fluorophore, respectively, were applied in postsynthetic "click"-type bioconjugation and coupled to oligonucleotides modified with alkyne groups using two alternative approaches: (i) as a nucleotide modification at the 2'-position of uridine and (ii) as a nucleotide substitution using (S)-(-)-3-amino-l,2-propanediol as an acyclic linker ...

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