On the stability of furanopyrimidin-2-one bases in oligonucleotides
Literature Information
Guan-Sheng Jiao, Kevin Burgess
The fluoresceinated furanopyrimidin-2-one nucleobase 4 incorporated into an oligonucleotide undergoes unexpectedly facile hydrolytic ring-opening in aqueous buffer at slightly elevated temperatures.
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![6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde structure 6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde structure](https://static.chemtradehub.com/structs/564/564-94-3-e746.webp)
![Ethyl 4-[8-chloro(5,5,6,6,7-~2~H_5_)-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene]-1-piperidinecarboxylate structure Ethyl 4-[8-chloro(5,5,6,6,7-~2~H_5_)-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene]-1-piperidinecarboxylate structure](https://static.chemtradehub.com/structs/102/1020719-57-6-37e2.webp)
