Collection Symposium Series
2011, 12, 304-306
https://doi.org/10.1135/css201112304
Published online 2015-08-20 10:11:49
Synthesis and reactions of 2,6-bis-(4-substituted-1,2,3-triazol-1-yl)-9-(β-D-arabinofuranosyl)purines
Armands Kovalovs, Māris Turks and Ērika Bizdēna
Individual author index pages
Other CCCC articles of these authors
- Māris Turks, Dace Katkevica, Helmars Smits and Ērika Bizdēna
A convenient synthesis of new sugar amino acid: 3-Aminomethyl-3-deoxy-1,2-O-isopropylidene-α-D-ribo-hexofuranuronic acid
Symposium Series 1999, Vol. 2, pp. 268–272 [Abstract]
Published online 2016-05-08 23:32:26 - Helmars Smits, Māris Turks, Dace Katkevica and Ērika Bizdēna
Synthesis of protected 3,5-dideoxy-3-C-azidomethyl-D-allofuranose, precursor of 3',5'-C-modified nucleoside analogs
Symposium Series 1999, Vol. 2, pp. 39–42 [Abstract]
Published online 2016-05-08 20:40:35 - Irina Novosjolova, Ērika Bizdēna, Ilona Mandrika, Ramona Petrovska, Jānis Kloviņš and Māris Turks
Biological activity profile of triazolylpurine nucleosides
Symposium Series 2014, Vol. 14, pp. 337–339 [Abstract]
Published online 2015-07-06 23:07:21 - Irina Novosjolova, Ērika Bizdēna and Māris Turks
Derivatives of 2,6-diazidopurine and 2,6-bis-(1,2,3-triazol-1-yl) purine as useful intermediates in the synthesis of modified purine nucleosides
Symposium Series 2014, Vol. 14, pp. 332–336 [Abstract]
Published online 2015-07-06 23:07:16 - Dace Cīrule, Kristers Ozols, Irina Novosjolova, Māris Turks and Ērika Bizdēna
A synthetic route to 2,6-bis-triazolyl purine deoxynucleosides via click chemistry
Symposium Series 2014, Vol. 14, pp. 233–235 [Abstract]
Published online 2015-07-06 23:02:44 - Andrejs Šišuļins, Irina Novosjolova, Māris Turks and Ērika Bizdēna
Synthesis of new fluorescent 9-alkyl-6-amino-2-triazolyl purines
Symposium Series 2014, Vol. 14, pp. 231–232 [Abstract]
Published online 2015-07-06 23:02:38 - Ērika Bizdēna, Eriks Rozners and Roger Strömberg
Synthesis and properties of 2'-O-methoxymethyl oligonucleotides
1996, Vol. 61, Special Issue, pp. S283–S286 [Abstract]