Snizhana Zaitseva

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Contact

Department of Chemistry
University of Basel
Mattenstrasse 24a, BPR-1096
4058 Basel
Switzerland

phone: +41 61 207 10 42
email: snizhana.zaitseva@clutterunibas.ch

Career

  • PhD student at the University of Basel (since October 2019)
  • Junior researcher, Russian Institute of Bioorganic Chemistry (2017-2019)
  • Master of Science, Department of Organic Chemistry, Peoples' Friendship University of Russia (2016-2018)
  • Bachelor of Science, Department of Technology of Pharmaceutical and Cosmetic Agents, D. Mendeleev University of Chemical Technology of Russia (2011-2015)

Publications

Design of red-shifted and environment-sensitive fluorogens based on GFP chromophore core
A. Yu. Smirnov, M. M. Perfilov, E. R. Zaitseva, M. B. Zagudaylova, S. O. Zaitseva, A. S. Mishin, M. S. Baranov
Dyes Pigments 2020, 177, 108258

Short duplex module coupled to G-quadruplexes increases fluorescence of synthetic GFP chromophore analogues
S. O. Zaitseva, N. S. Baleeva, T. S. Zatsepin, I. N. Myasnyanko, A. V. Turaev, G. E. Pozmogova, A. A. Khrulev, A. M. Varizhuk, M. S. Baranov, A. V. Aralov
Sensors 2020, 20(3), 915

Red-shifted substrates for FAST fluorogen-activating protein based on the GFP-like chromophores
N. V. Povarova, S. O. Zaitseva, N. S. Baleeva, A. Yu. Smirnov, I. N. Myasnyanko, M. B. Zagudaylova, N. G. Bozhanova, D. A. Gorbachev, K. K. Malyshevskaya, A. S. Gavrikov, A. S. Mishin, M.S. Baranov Chem. Eur. J. 2019 25 , 9592-2596

Designing redder and brighter fluorophores by synergistic tuning of ground and excited states
C. Chen, M. S. Baranov, L. Zhu, N. S. Baleeva, A. Y. Smirnov, S. O. Zaitseva, I. V. Yampolsky, K. V. Solntsev, C. Fang
Chem. Commun. 2019, 55, 2537-2540

Enamine–azide [2+3]-cycloaddition as a method to introduce functional groups into fluorescent dyes
N. S. Baleeva, S. O. Zaitseva , K. S. Mineev, A. V. Khavroshechkina , M. B. Zagudaylova, M. S. Baranov
Tetrahedron Lett. 2019, 60, 456-459

Synthesis of the new green fluorescent protein chromophore analogue starting from the cinnamic aldehyde derivativeS. O. Zaitseva, M. S. BaranovRuss.J. Bioorg. Chem. 2019, 45, 214-216

Azidoacetic acid amides in the synthesis of substituted arylidene-1-H-imidazol-5-(4H)-ones
S. O. Zaitseva, S. V. Golodukhina, N. S. Baleeva , E. A. Levina , A. Y. Smirnov, M. B. Zagudaylova, M. S. Baranov
ChemistrySelect 2018, 3, 8593-8596

Homophthalonitrile for multicomponent reactions: Syntheses and optical properties of o‐cyanophenyl‐ or indol‐3‐yl‐substituted chromeno[2,3‐c]isoquinolin‐5‐amines
A. A. Festa, O. A. Storozhenko, N. E. Golantsov, K. Subramani, R. A. Novikov, S. O. Zaitseva, M. S. Baranov, A. V. Varlamov, L. G. Voskressensky
ChemistryOpen 2018, 8, 23-30

Derivatives of azidocinnamic acid in the synthesis of 2-amino-4-arylidene-1H-imidazol-5(4H)-ones
A.Y. Smirnov, N. S. Baleeva, S. O. Zaitseva, K. S. Mineev, M. S. Baranov
Chem. Heterocycl. Compd. 2018, 54, 625

The role of N-substituents in radiationless deactivation of aminated derivatives of a locked GFP chromophore
N. S. Baleeva, S. O. Zaitseva, D. A. Gorbachev, A. Y. Smirnov, M. B. Zagudaylova, M. S. Baranov
Eur. J. Org. Chem. 2017, 35, 5219-5224