Novel Fluorescent Purine Nucleoside-Amino Acid Conjugates
XXII International Round Table on Nucleosides, Nucleotides and Nucleic Acids: Abstract Book 2016
Dace Cīrule, Kristers Ozols, oskars Platnieks, Ērika Bizdēna, Māris Turks

Our group has recently reported the synthesis of 2,6-bis-triazolyl purine nucleosides and their regioselective reactions with primary and secondary amines and thiols. The obtained N6- substituted 2-triazolyl adenosine analogs possessed good fluorescent properties. Thus, we proceeded to investigate purine nucleoside SNAr chemistry which uses 1,2,3-triazole as a leaving group and to study photophysical properties of the obtained purine nucleoside-amino acid adducts.


Keywords
Purine, Nucleosides, Nucleoside-amino acid conjugates, Click chemistry, Fluorescence

Cīrule, D., Ozols, K., Platnieks, O., Bizdēna, Ē., Turks, M. Novel Fluorescent Purine Nucleoside-Amino Acid Conjugates. In: XXII International Round Table on Nucleosides, Nucleotides and Nucleic Acids: Abstract Book, France, Paris, 18-22 July, 2016. Paris: 2016, pp.215-216.

Publication language
English (en)
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