Fomich M. A., Kvach M. V., Navakouski M. J., Weise C., Baranovsky A. V., Korshun V. A., Shmanai V. V.
Azide Phosphoramidite in Direct Synthesis of Azide-Modified Oligonucleotides
V.I.Potkin, D.Shcharbin, A.A.Denisov, S.G.Paschkevich, M.Bryszewska, S.K.Petkevich, A.V.Kletskov, D.O.Lapotko, V.V.Kazbanov, T.A.Gurinovich, V.A.Kulchitsky
The influence of heterocyclic compound-PAMAM dendrimer complexes on evoked electrical responses in slices of hypoxic brain tissue
Yu.G. Yegiazarov, M.F. Gorbatsevich, Ye.N. Yermolenko, L.L. Potapova, A.Yu. Volodin, B.Kh. Cherches, A.A. Shunkevich, V.V. Korotkevich
Effect of the Distribution of Palladium over the Cross Section of an Ion-Exchanger Fiber on Catalyst Activity in a Water Deoxygenation Process
Potkin V.I., Petkevich S.K., Kurman P.V., Levkovskaya G.G., Ivashkevich L.S., Lyakhov A.S.
Bimolecular condensation of 1-(para-tolyl)- and 1-(biphenyl-4-yl)-3,4,4-trichloro-3-buten-1-ones to 2,3,4,6-substituted 4Н-pyrans
Azide and phosphoramidite functions were found to be compatible within one molecule and stable for months in solution kept frozen at −20 °C. An azide-carrying phosphoramidite was used for direct introduction of multiple azide modifications into synthetic oligonucleotides. A series of azide-containing oligonucleotides were modified further using click reactions with alkynes.
Organic Letters 2014, 16 (17), 4590–4593
© 2009 INSTITUTE OF PHYSICAL ORGANIC CHEMISTRY OF NASB
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